Canonical Allele Identifier: CA1925788216
Gene: GLUD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87053404C= , CM000672.2:g.87053404C= GRCh38
NC_000010.10:g.88813161C= , CM000672.1:g.88813161C= GRCh37
NC_000010.9:g.88803141C= NCBI36
NG_013010.1:g.46616G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474574.2:n.3070G=
ENST00000487058.2:n.1242G=
ENST00000681987.1:n.1333G=
ENST00000681988.1:c.994G= ENSP00000507316.1:p.Gly332=
ENST00000682396.1:c.1486G= ENSP00000506764.1:n.1486G=
ENST00000682507.1:c.994G= ENSP00000508098.1:p.Gly332=
ENST00000682622.1:c.1775G= ENSP00000506732.1:n.1775G=
ENST00000682833.1:c.1330G=
ENST00000683022.1:c.1516G=
ENST00000683256.1:c.994G= ENSP00000507901.1:p.Gly332=
ENST00000683269.1:c.994G= ENSP00000508107.1:p.Gly332=
ENST00000683647.1:n.4829G=
ENST00000683649.1:n.345G=
ENST00000683783.1:c.994G= ENSP00000507881.1:p.Gly332=
ENST00000683813.1:n.1223G=
ENST00000684032.1:c.1350G= ENSP00000506969.1:n.1350G=
ENST00000684201.1:c.1219G= ENSP00000507887.1:p.Gly407=
ENST00000684338.1:c.1495G= ENSP00000507457.1:p.Gly499=
ENST00000684372.1:c.994G= ENSP00000508244.1:p.Gly332=
ENST00000684434.1:c.966G=
ENST00000684546.1:c.994G= ENSP00000507729.1:p.Gly332=
ENST00000684665.1:n.459G=
ENST00000684690.1:n.1722G=
ENST00000684699.1:n.4074G=
ENST00000277865.5:c.1495G= MANE Select ENSP00000277865.4:p.Gly499=
ENST00000277865.4:c.1495G= ENSP00000277865.4:p.Gly499=
NM_005271.3:c.1495G= NP_005262.1:p.Gly499=
XM_011539668.1:c.994G= XP_011537970.1:p.Gly332=
XM_011539669.1:c.994G= XP_011537971.1:p.Gly332=
NM_001318900.1:c.1096G= NP_001305829.1:p.Gly366=
NM_001318901.1:c.994G= NP_001305830.1:p.Gly332=
NM_001318902.1:c.994G= NP_001305831.1:p.Gly332=
NM_001318904.1:c.994G= NP_001305833.1:p.Gly332=
NM_001318905.1:c.994G= NP_001305834.1:p.Gly332=
NM_001318906.1:c.994G= NP_001305835.1:p.Gly332=
NM_005271.4:c.1495G= NP_005262.1:p.Gly499=
NM_005271.5:c.1495G= MANE Select NP_005262.1:p.Gly499=
NM_001318904.2:c.994G= NP_001305833.1:p.Gly332=
NM_001318905.2:c.994G= NP_001305834.1:p.Gly332=
NM_001318906.2:c.994G= NP_001305835.1:p.Gly332=