Canonical Allele Identifier: CA1307083866
Gene: GAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.170837125T= , CM000664.2:g.170837125T= GRCh38
NC_000002.11:g.171693635T= , CM000664.1:g.171693635T= GRCh37
NC_000002.10:g.171401881T= NCBI36
NG_021477.1:g.25436T=

Transcript Alleles

HGVS Amino-acid change
ENST00000358196.8:c.638+242T= MANE Select ENSP00000350928.3:n.638+242T=
ENST00000344257.9:c.638+242T= ENSP00000341167.5:n.638+242T=
ENST00000358196.7:c.638+242T= ENSP00000350928.3:n.638+242T=
ENST00000375272.5:c.638+242T= ENSP00000364421.1:n.638+242T=
ENST00000414527.6:c.638+242T= ENSP00000403849.1:n.638+242T=
ENST00000429023.1:n.619+242T=
ENST00000493875.5:c.638+242T= ENSP00000434696.1:n.638+242T=
ENST00000625689.2:c.638+242T= ENSP00000486612.1:n.638+242T=
NM_000817.2:c.638+242T= NP_000808.2:n.638+242T=
NM_013445.3:c.638+242T= NP_038473.2:n.638+242T=
XM_005246444.2:c.638+242T= XP_005246501.1:n.638+242T=
XM_011510922.1:c.638+242T= XP_011509224.1:n.638+242T=
XM_005246444.3:c.638+242T= XP_005246501.1:n.638+242T=
XM_017003756.1:c.638+242T= XP_016859245.1:n.638+242T=
XM_017003757.2:c.638+242T= XP_016859246.1:n.638+242T=
XM_017003758.2:c.638+242T= XP_016859247.1:n.638+242T=
NM_000817.3:c.638+242T= MANE Select NP_000808.2:n.638+242T=
NM_013445.4:c.638+242T= NP_038473.2:n.638+242T=