Canonical Allele Identifier: CA1307071366

Gene: GAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.170818626C= , CM000664.2:g.170818626C=	GRCh38
NC_000002.11:g.171675136C= , CM000664.1:g.171675136C=	GRCh37
NC_000002.10:g.171383382C=	NCBI36
NG_021477.1:g.6937C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000817.3:c.35C= MANE Select	NP_000808.2:p.Ser12=
ENST00000358196.8:c.35C= MANE Select	ENSP00000350928.3:p.Ser12=
NM_000817.2:c.35C=	NP_000808.2:p.Ser12=
NM_013445.3:c.35C=	NP_038473.2:p.Ser12=
NM_013445.4:c.35C=	NP_038473.2:p.Ser12=
ENST00000344257.9:c.35C=	ENSP00000341167.5:p.Ser12=
ENST00000358196.7:c.35C=	ENSP00000350928.3:p.Ser12=
ENST00000375272.5:c.35C=	ENSP00000364421.1:p.Ser12=
ENST00000414527.6:c.35C=	ENSP00000403849.1:p.Ser12=
ENST00000429023.1:n.16C=
ENST00000445006.5:c.35C=	ENSP00000394948.1:p.Ser12=
ENST00000454603.5:c.35C=	ENSP00000402366.1:p.Ser12=
ENST00000455008.5:c.35C=	ENSP00000405917.1:p.Ser12=
ENST00000456864.5:c.35C=	ENSP00000394255.1:p.Ser12=
ENST00000493875.5:c.35C=	ENSP00000434696.1:p.Ser12=
ENST00000625689.2:c.35C=	ENSP00000486612.1:p.Ser12=
XM_005246444.2:c.35C=	XP_005246501.1:p.Ser12=
XM_005246444.3:c.35C=	XP_005246501.1:p.Ser12=
XM_011510922.1:c.35C=	XP_011509224.1:p.Ser12=
XM_017003756.1:c.35C=	XP_016859245.1:p.Ser12=
XM_017003757.2:c.35C=	XP_016859246.1:p.Ser12=
XM_017003758.2:c.35C=	XP_016859247.1:p.Ser12=