Canonical Allele Identifier: CA1307078386
Gene: GAD1 HGNC NCBI

Linked Data

dbSNP Id: rs3828275

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.170826230C>A , CM000664.2:g.170826230C>A GRCh38
NC_000002.11:g.171682740C>A , CM000664.1:g.171682740C>A GRCh37
NC_000002.10:g.171390986C>A NCBI36
NG_021477.1:g.14541C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358196.8:c.146-3245C>A MANE Select ENSP00000350928.3:n.146-3245C>A
ENST00000344257.9:c.146-3245C>A ENSP00000341167.5:n.146-3245C>A
ENST00000358196.7:c.146-3245C>A ENSP00000350928.3:n.146-3245C>A
ENST00000375272.5:c.146-3245C>A ENSP00000364421.1:n.146-3245C>A
ENST00000414527.6:c.146-3245C>A ENSP00000403849.1:n.146-3245C>A
ENST00000429023.1:n.127-3245C>A
ENST00000454603.5:c.146-3245C>A ENSP00000402366.1:n.146-3245C>A
ENST00000455008.5:c.146-3245C>A ENSP00000405917.1:n.146-3245C>A
ENST00000456864.5:c.146-3245C>A ENSP00000394255.1:n.146-3245C>A
ENST00000485013.1:n.433-3245C>A
ENST00000486850.1:c.64-3245C>A
ENST00000493875.5:c.146-3245C>A ENSP00000434696.1:n.146-3245C>A
ENST00000625689.2:c.146-3245C>A ENSP00000486612.1:n.146-3245C>A
NM_000817.2:c.146-3245C>A NP_000808.2:n.146-3245C>A
NM_013445.3:c.146-3245C>A NP_038473.2:n.146-3245C>A
XM_005246444.2:c.146-3245C>A XP_005246501.1:n.146-3245C>A
XM_011510922.1:c.146-3245C>A XP_011509224.1:n.146-3245C>A
XM_005246444.3:c.146-3245C>A XP_005246501.1:n.146-3245C>A
XM_017003756.1:c.146-3245C>A XP_016859245.1:n.146-3245C>A
XM_017003757.2:c.146-3245C>A XP_016859246.1:n.146-3245C>A
XM_017003758.2:c.146-3245C>A XP_016859247.1:n.146-3245C>A
NM_000817.3:c.146-3245C>A MANE Select NP_000808.2:n.146-3245C>A
NM_013445.4:c.146-3245C>A NP_038473.2:n.146-3245C>A