ClinVar

NM_001127222.2(CACNA1A):c.6466C>T (p.Arg2156Cys)

Gene:

CACNA1A:calcium voltage-gated channel subunit alpha1 A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.13

Genomic location:

• Chr19: 13209372 (on Assembly GRCh38)
• Chr19: 13320186 (on Assembly GRCh37)

Preferred name:

NM_001127222.2(CACNA1A):c.6466C>T (p.Arg2156Cys)

HGVS:

• NC_000019.10:g.13209372G>A
• NG_011569.1:g.302089C>T
• NM_000068.4:c.6484C>T
• NM_001127221.2:c.6469C>T
• NM_001127222.1:c.6466C>T
• NM_001127222.2:c.6466C>TMANE SELECT
• NM_001174080.2:c.6475C>T
• NM_023035.3:c.6484C>T
• NP_000059.3:p.Arg2162Cys
• NP_001120693.1:p.Arg2157Cys
• NP_001120693.1:p.Arg2157Cys
• NP_001120694.1:p.Arg2156Cys
• NP_001167551.1:p.Arg2159Cys
• NP_075461.2:p.Arg2162Cys
• LRG_7t1:c.6469C>T
• LRG_7:g.302089C>T
• LRG_7p1:p.Arg2157Cys
• NC_000019.9:g.13320186G>A
• NM_001127221.1:c.6469C>T
• NM_001127221.2:c.6469C>T

This HGVS expression did not pass validation

Protein change:

R2156C

Links:

dbSNP: rs554393704

Molecular consequence:

• NM_000068.4:c.6484C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127221.2:c.6469C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127222.2:c.6466C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001174080.2:c.6475C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_023035.3:c.6484C>T - missense variant - [Sequence Ontology: SO:0001583]