Canonical Allele Identifier: CA1307085842

Gene: GAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.170842162T= , CM000664.2:g.170842162T=	GRCh38
NC_000002.11:g.171698672T= , CM000664.1:g.171698672T=	GRCh37
NC_000002.10:g.171406918T=	NCBI36
NG_021477.1:g.30473T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358196.8:c.639-1883T= MANE Select	ENSP00000350928.3:n.639-1883T=
ENST00000344257.9:c.639-407T=	ENSP00000341167.5:n.639-407T=
ENST00000358196.7:c.639-1883T=	ENSP00000350928.3:n.639-1883T=
ENST00000375272.5:c.639-407T=	ENSP00000364421.1:n.639-407T=
ENST00000414527.6:c.639-3344T=	ENSP00000403849.1:n.639-3344T=
ENST00000429023.1:n.620-407T=
ENST00000493875.5:c.639-1883T=	ENSP00000434696.1:n.639-1883T=
ENST00000625689.2:c.639-1883T=	ENSP00000486612.1:n.639-1883T=
NM_000817.2:c.639-1883T=	NP_000808.2:n.639-1883T=
NM_013445.3:c.639-407T=	NP_038473.2:n.639-407T=
XM_005246444.2:c.639-407T=	XP_005246501.1:n.639-407T=
XM_011510922.1:c.639-1883T=	XP_011509224.1:n.639-1883T=
XM_005246444.3:c.639-407T=	XP_005246501.1:n.639-407T=
XM_017003756.1:c.639-1883T=	XP_016859245.1:n.639-1883T=
XM_017003757.2:c.639-1883T=	XP_016859246.1:n.639-1883T=
XM_017003758.2:c.639-407T=	XP_016859247.1:n.639-407T=
NM_000817.3:c.639-1883T= MANE Select	NP_000808.2:n.639-1883T=
NM_013445.4:c.639-407T=	NP_038473.2:n.639-407T=