Canonical Allele Identifier: CA1925791430
Gene: GLUD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87060743G= , CM000672.2:g.87060743G= GRCh38
NC_000010.10:g.88820500G= , CM000672.1:g.88820500G= GRCh37
NC_000010.9:g.88810480G= NCBI36
NG_013010.1:g.39277C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474574.2:n.2717C=
ENST00000487058.2:n.443C=
ENST00000681987.1:n.980C=
ENST00000681988.1:c.641C= ENSP00000507316.1:p.Pro214=
ENST00000682396.1:c.1133C= ENSP00000506764.1:n.1133C=
ENST00000682507.1:c.641C= ENSP00000508098.1:p.Pro214=
ENST00000682622.1:c.1422C= ENSP00000506732.1:n.1422C=
ENST00000682833.1:c.977C=
ENST00000683022.1:c.1163C=
ENST00000683256.1:c.641C= ENSP00000507901.1:p.Pro214=
ENST00000683269.1:c.641C= ENSP00000508107.1:p.Pro214=
ENST00000683647.1:n.4476C=
ENST00000683783.1:c.641C= ENSP00000507881.1:p.Pro214=
ENST00000683813.1:n.870C=
ENST00000684032.1:c.997C= ENSP00000506969.1:n.997C=
ENST00000684201.1:c.922-502C= ENSP00000507887.1:n.922-502C=
ENST00000684338.1:c.1142C= ENSP00000507457.1:p.Pro381=
ENST00000684372.1:c.641C= ENSP00000508244.1:p.Pro214=
ENST00000684392.1:n.1873C=
ENST00000684434.1:c.613C=
ENST00000684546.1:c.641C= ENSP00000507729.1:p.Pro214=
ENST00000684690.1:n.923C=
ENST00000684699.1:n.3275C=
ENST00000277865.5:c.1142C= MANE Select ENSP00000277865.4:p.Pro381=
ENST00000277865.4:c.1142C= ENSP00000277865.4:p.Pro381=
ENST00000465164.1:n.221C=
NM_005271.3:c.1142C= NP_005262.1:p.Pro381=
XM_011539668.1:c.641C= XP_011537970.1:p.Pro214=
XM_011539669.1:c.641C= XP_011537971.1:p.Pro214=
NM_001318900.1:c.743C= NP_001305829.1:p.Pro248=
NM_001318901.1:c.641C= NP_001305830.1:p.Pro214=
NM_001318902.1:c.641C= NP_001305831.1:p.Pro214=
NM_001318904.1:c.641C= NP_001305833.1:p.Pro214=
NM_001318905.1:c.641C= NP_001305834.1:p.Pro214=
NM_001318906.1:c.641C= NP_001305835.1:p.Pro214=
NM_005271.4:c.1142C= NP_005262.1:p.Pro381=
NM_005271.5:c.1142C= MANE Select NP_005262.1:p.Pro381=
NM_001318904.2:c.641C= NP_001305833.1:p.Pro214=
NM_001318905.2:c.641C= NP_001305834.1:p.Pro214=
NM_001318906.2:c.641C= NP_001305835.1:p.Pro214=