Canonical Allele Identifier: CA079574
Community Standard Title: NM_000069.3(CACNA1S):c.3166A>G (p.Met1056Val)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201061356T>C , CM000663.2:g.201061356T>C GRCh38
NC_000001.10:g.201030484T>C , CM000663.1:g.201030484T>C GRCh37
NC_000001.9:g.199297107T>C NCBI36
NG_009816.1:g.56211A>G
NG_009816.2:g.56211A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.3166A>G MANE Select NP_000060.2:p.Met1056Val
ENST00000362061.4:c.3166A>G MANE Select ENSP00000355192.3:p.Met1056Val
NM_000069.2:c.3166A>G NP_000060.2:p.Met1056Val
ENST00000362061.3:c.3166A>G ENSP00000355192.3:p.Met1056Val
ENST00000367338.7:c.3166A>G ENSP00000356307.3:p.Met1056Val
ENST00000679417.1:c.*2329A>G ENSP00000506706.1:n.*2329A>G
ENST00000680051.1:n.292A>G
ENST00000680059.1:c.*684A>G ENSP00000504944.1:n.*684A>G
ENST00000681078.1:c.3166A>G ENSP00000506645.1:p.Met1056Val
ENST00000681190.1:c.3166A>G ENSP00000506428.1:p.Met1056Val
ENST00000681874.1:c.3106A>G ENSP00000505162.1:p.Met1036Val
XM_005245478.2:c.3166A>G XP_005245535.1:p.Met1056Val
XM_005245478.3:c.3166A>G XP_005245535.1:p.Met1056Val