Canonical Allele Identifier: CA082550
Community Standard Title: NM_000069.3(CACNA1S):c.3425A>G (p.Gln1142Arg)
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201059289T>C , CM000663.2:g.201059289T>C GRCh38
NC_000001.10:g.201028417T>C , CM000663.1:g.201028417T>C GRCh37
NC_000001.9:g.199295040T>C NCBI36
NG_009816.1:g.58278A>G
NG_009816.2:g.58278A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.3425A>G MANE Select NP_000060.2:p.Gln1142Arg
ENST00000362061.4:c.3425A>G MANE Select ENSP00000355192.3:p.Gln1142Arg
NM_000069.2:c.3425A>G NP_000060.2:p.Gln1142Arg
ENST00000362061.3:c.3425A>G ENSP00000355192.3:p.Gln1142Arg
ENST00000367338.7:c.3425A>G ENSP00000356307.3:p.Gln1142Arg
ENST00000679417.1:c.*2588A>G ENSP00000506706.1:n.*2588A>G
ENST00000680051.1:n.551A>G
ENST00000680059.1:c.*943A>G ENSP00000504944.1:n.*943A>G
ENST00000681078.1:c.3425A>G ENSP00000506645.1:p.Gln1142Arg
ENST00000681190.1:c.3425A>G ENSP00000506428.1:p.Gln1142Arg
ENST00000681874.1:c.3365A>G ENSP00000505162.1:p.Gln1122Arg
XM_005245478.2:c.3425A>G XP_005245535.1:p.Gln1142Arg
XM_005245478.3:c.3425A>G XP_005245535.1:p.Gln1142Arg