Canonical Allele Identifier: CA11166719

Gene: GAD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.170836945A>C , CM000664.2:g.170836945A>C	GRCh38
NC_000002.11:g.171693455A>C , CM000664.1:g.171693455A>C	GRCh37
NC_000002.10:g.171401701A>C	NCBI36
NG_021477.1:g.25256A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358196.8:c.638+62A>C MANE Select	ENSP00000350928.3:n.638+62A>C
ENST00000344257.9:c.638+62A>C	ENSP00000341167.5:n.638+62A>C
ENST00000358196.7:c.638+62A>C	ENSP00000350928.3:n.638+62A>C
ENST00000375272.5:c.638+62A>C	ENSP00000364421.1:n.638+62A>C
ENST00000414527.6:c.638+62A>C	ENSP00000403849.1:n.638+62A>C
ENST00000429023.1:n.619+62A>C
ENST00000493875.5:c.638+62A>C	ENSP00000434696.1:n.638+62A>C
ENST00000625689.2:c.638+62A>C	ENSP00000486612.1:n.638+62A>C
NM_000817.2:c.638+62A>C	NP_000808.2:n.638+62A>C
NM_013445.3:c.638+62A>C	NP_038473.2:n.638+62A>C
XM_005246444.2:c.638+62A>C	XP_005246501.1:n.638+62A>C
XM_011510922.1:c.638+62A>C	XP_011509224.1:n.638+62A>C
XM_005246444.3:c.638+62A>C	XP_005246501.1:n.638+62A>C
XM_017003756.1:c.638+62A>C	XP_016859245.1:n.638+62A>C
XM_017003757.2:c.638+62A>C	XP_016859246.1:n.638+62A>C
XM_017003758.2:c.638+62A>C	XP_016859247.1:n.638+62A>C
NM_000817.3:c.638+62A>C MANE Select	NP_000808.2:n.638+62A>C
NM_013445.4:c.638+62A>C	NP_038473.2:n.638+62A>C