Canonical Allele Identifier: CA079429
Community Standard Title: NM_000069.3(CACNA1S):c.2932G>A (p.Gly978Arg)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201062065C>T , CM000663.2:g.201062065C>T GRCh38
NC_000001.10:g.201031193C>T , CM000663.1:g.201031193C>T GRCh37
NC_000001.9:g.199297816C>T NCBI36
NG_009816.1:g.55502G>A
NG_009816.2:g.55502G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.2932G>A MANE Select NP_000060.2:p.Gly978Arg
ENST00000362061.4:c.2932G>A MANE Select ENSP00000355192.3:p.Gly978Arg
NM_000069.2:c.2932G>A NP_000060.2:p.Gly978Arg
ENST00000362061.3:c.2932G>A ENSP00000355192.3:p.Gly978Arg
ENST00000367338.7:c.2932G>A ENSP00000356307.3:p.Gly978Arg
ENST00000679417.1:c.*2095G>A ENSP00000506706.1:n.*2095G>A
ENST00000680051.1:n.58G>A
ENST00000680059.1:c.*450G>A ENSP00000504944.1:n.*450G>A
ENST00000681078.1:c.2932G>A ENSP00000506645.1:p.Gly978Arg
ENST00000681190.1:c.2932G>A ENSP00000506428.1:p.Gly978Arg
ENST00000681874.1:c.2872G>A ENSP00000505162.1:p.Gly958Arg
XM_005245478.2:c.2932G>A XP_005245535.1:p.Gly978Arg
XM_005245478.3:c.2932G>A XP_005245535.1:p.Gly978Arg