Canonical Allele Identifier: CA079145
Community Standard Title: NM_000069.3(CACNA1S):c.2630C>T (p.Ala877Val)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201066914G>A , CM000663.2:g.201066914G>A GRCh38
NC_000001.10:g.201036042G>A , CM000663.1:g.201036042G>A GRCh37
NC_000001.9:g.199302665G>A NCBI36
NG_009816.1:g.50653C>T
NG_009816.2:g.50653C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.2630C>T MANE Select NP_000060.2:p.Ala877Val
ENST00000362061.4:c.2630C>T MANE Select ENSP00000355192.3:p.Ala877Val
NM_000069.2:c.2630C>T NP_000060.2:p.Ala877Val
ENST00000362061.3:c.2630C>T ENSP00000355192.3:p.Ala877Val
ENST00000367338.7:c.2630C>T ENSP00000356307.3:p.Ala877Val
ENST00000679417.1:c.*1793C>T ENSP00000506706.1:n.*1793C>T
ENST00000680059.1:c.*148C>T ENSP00000504944.1:n.*148C>T
ENST00000681078.1:c.2630C>T ENSP00000506645.1:p.Ala877Val
ENST00000681190.1:c.2630C>T ENSP00000506428.1:p.Ala877Val
ENST00000681874.1:c.2570C>T ENSP00000505162.1:p.Ala857Val
XM_005245478.2:c.2630C>T XP_005245535.1:p.Ala877Val
XM_005245478.3:c.2630C>T XP_005245535.1:p.Ala877Val