Canonical Allele Identifier: CA1925791505
Gene: GLUD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87060947T= , CM000672.2:g.87060947T= GRCh38
NC_000010.10:g.88820704T= , CM000672.1:g.88820704T= GRCh37
NC_000010.9:g.88810684T= NCBI36
NG_013010.1:g.39073A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474574.2:n.2602A=
ENST00000487058.2:n.239A=
ENST00000681987.1:n.865A=
ENST00000681988.1:c.526A= ENSP00000507316.1:p.Ile176=
ENST00000682396.1:c.1018A= ENSP00000506764.1:n.1018A=
ENST00000682507.1:c.526A= ENSP00000508098.1:p.Ile176=
ENST00000682622.1:c.1307A= ENSP00000506732.1:n.1307A=
ENST00000682833.1:c.862A=
ENST00000683022.1:c.1048A=
ENST00000683256.1:c.526A= ENSP00000507901.1:p.Ile176=
ENST00000683269.1:c.526A= ENSP00000508107.1:p.Ile176=
ENST00000683647.1:n.4361A=
ENST00000683783.1:c.526A= ENSP00000507881.1:p.Ile176=
ENST00000683813.1:n.755A=
ENST00000684032.1:c.882A= ENSP00000506969.1:n.882A=
ENST00000684201.1:c.922-706A= ENSP00000507887.1:n.922-706A=
ENST00000684338.1:c.1027A= ENSP00000507457.1:p.Ile343=
ENST00000684372.1:c.526A= ENSP00000508244.1:p.Ile176=
ENST00000684392.1:n.1758A=
ENST00000684434.1:c.498A=
ENST00000684546.1:c.526A= ENSP00000507729.1:p.Ile176=
ENST00000684690.1:n.808A=
ENST00000684699.1:n.3160A=
ENST00000277865.5:c.1027A= MANE Select ENSP00000277865.4:p.Ile343=
ENST00000277865.4:c.1027A= ENSP00000277865.4:p.Ile343=
ENST00000465164.1:n.106A=
NM_005271.3:c.1027A= NP_005262.1:p.Ile343=
XM_011539668.1:c.526A= XP_011537970.1:p.Ile176=
XM_011539669.1:c.526A= XP_011537971.1:p.Ile176=
NM_001318900.1:c.628A= NP_001305829.1:p.Ile210=
NM_001318901.1:c.526A= NP_001305830.1:p.Ile176=
NM_001318902.1:c.526A= NP_001305831.1:p.Ile176=
NM_001318904.1:c.526A= NP_001305833.1:p.Ile176=
NM_001318905.1:c.526A= NP_001305834.1:p.Ile176=
NM_001318906.1:c.526A= NP_001305835.1:p.Ile176=
NM_005271.4:c.1027A= NP_005262.1:p.Ile343=
NM_005271.5:c.1027A= MANE Select NP_005262.1:p.Ile343=
NM_001318904.2:c.526A= NP_001305833.1:p.Ile176=
NM_001318905.2:c.526A= NP_001305834.1:p.Ile176=
NM_001318906.2:c.526A= NP_001305835.1:p.Ile176=