Canonical Allele Identifier: CA10611332

Gene: GAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.170816965G>A , CM000664.2:g.170816965G>A	GRCh38
NC_000002.11:g.171673475G>A , CM000664.1:g.171673475G>A	GRCh37
NC_000002.10:g.171381721G>A	NCBI36
NG_021477.1:g.5276G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358196.8:c.-147G>A MANE Select	ENSP00000350928.3:n.-147G>A
ENST00000344257.9:c.-147G>A	ENSP00000341167.5:n.-147G>A
ENST00000358196.7:c.-147G>A	ENSP00000350928.3:n.-147G>A
ENST00000375272.5:c.-151G>A	ENSP00000364421.1:n.-151G>A
ENST00000445006.5:c.-147G>A	ENSP00000394948.1:n.-147G>A
ENST00000454603.5:c.-63-1564G>A	ENSP00000402366.1:n.-63-1564G>A
ENST00000625689.2:c.-147G>A	ENSP00000486612.1:n.-147G>A
NM_000817.2:c.-147G>A	NP_000808.2:n.-147G>A
NM_013445.3:c.-151G>A	NP_038473.2:n.-151G>A
XM_005246444.2:c.-147G>A	XP_005246501.1:n.-147G>A
XM_011510922.1:c.-63-1564G>A	XP_011509224.1:n.-63-1564G>A
XM_005246444.3:c.-147G>A	XP_005246501.1:n.-147G>A
XM_017003757.2:c.-147G>A	XP_016859246.1:n.-147G>A
XM_017003758.2:c.-147G>A	XP_016859247.1:n.-147G>A
NM_000817.3:c.-147G>A MANE Select	NP_000808.2:n.-147G>A
NM_013445.4:c.-151G>A	NP_038473.2:n.-151G>A