Canonical Allele Identifier: CA422719429
Community Standard Title: NM_000069.3(CACNA1S):c.3885G>A (p.Val1295=)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201052625C>T , CM000663.2:g.201052625C>T GRCh38
NC_000001.10:g.201021753C>T , CM000663.1:g.201021753C>T GRCh37
NC_000001.9:g.199288376C>T NCBI36
NG_009816.1:g.64942G>A
NG_009816.2:g.64942G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.3885G>A MANE Select NP_000060.2:p.Val1295=
ENST00000362061.4:c.3885G>A MANE Select ENSP00000355192.3:p.Val1295=
NM_000069.2:c.3885G>A NP_000060.2:p.Val1295=
ENST00000362061.3:c.3885G>A ENSP00000355192.3:p.Val1295=
ENST00000367338.7:c.3828G>A ENSP00000356307.3:p.Val1276=
ENST00000679417.1:c.*3048G>A ENSP00000506706.1:n.*3048G>A
ENST00000680051.1:n.1011G>A
ENST00000680059.1:c.*1403G>A ENSP00000504944.1:n.*1403G>A
ENST00000681078.1:c.3885G>A ENSP00000506645.1:p.Val1295=
ENST00000681190.1:c.*67G>A ENSP00000506428.1:n.*67G>A
ENST00000681874.1:c.3825G>A ENSP00000505162.1:p.Val1275=
XM_005245478.2:c.3828G>A XP_005245535.1:p.Val1276=
XM_005245478.3:c.3828G>A XP_005245535.1:p.Val1276=