Canonical Allele Identifier: CA152995

Gene: GLUD1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87057715C>T , CM000672.2:g.87057715C>T	GRCh38
NC_000010.10:g.88817472C>T , CM000672.1:g.88817472C>T	GRCh37
NC_000010.9:g.88807452C>T	NCBI36
NG_013010.1:g.42305G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474574.2:n.3045G>A
ENST00000487058.2:n.1217G>A
ENST00000681987.1:n.1308G>A
ENST00000681988.1:c.969G>A	ENSP00000507316.1:p.Thr323=
ENST00000682396.1:c.1461G>A	ENSP00000506764.1:n.1461G>A
ENST00000682507.1:c.969G>A	ENSP00000508098.1:p.Thr323=
ENST00000682622.1:c.1750G>A	ENSP00000506732.1:n.1750G>A
ENST00000682833.1:c.1305G>A
ENST00000683022.1:c.1491G>A
ENST00000683256.1:c.969G>A	ENSP00000507901.1:p.Thr323=
ENST00000683269.1:c.969G>A	ENSP00000508107.1:p.Thr323=
ENST00000683647.1:n.4804G>A
ENST00000683649.1:n.320G>A
ENST00000683783.1:c.969G>A	ENSP00000507881.1:p.Thr323=
ENST00000683813.1:n.1198G>A
ENST00000684032.1:c.1325G>A	ENSP00000506969.1:n.1325G>A
ENST00000684201.1:c.1194G>A	ENSP00000507887.1:p.Thr398=
ENST00000684338.1:c.1470G>A	ENSP00000507457.1:p.Thr490=
ENST00000684372.1:c.969G>A	ENSP00000508244.1:p.Thr323=
ENST00000684434.1:c.941G>A
ENST00000684546.1:c.969G>A	ENSP00000507729.1:p.Thr323=
ENST00000684690.1:n.1697G>A
ENST00000684699.1:n.4049G>A
ENST00000277865.5:c.1470G>A MANE Select	ENSP00000277865.4:p.Thr490=
ENST00000277865.4:c.1470G>A	ENSP00000277865.4:p.Thr490=
NM_005271.3:c.1470G>A	NP_005262.1:p.Thr490=
XM_011539668.1:c.969G>A	XP_011537970.1:p.Thr323=
XM_011539669.1:c.969G>A	XP_011537971.1:p.Thr323=
NM_001318900.1:c.1071G>A	NP_001305829.1:p.Thr357=
NM_001318901.1:c.969G>A	NP_001305830.1:p.Thr323=
NM_001318902.1:c.969G>A	NP_001305831.1:p.Thr323=
NM_001318904.1:c.969G>A	NP_001305833.1:p.Thr323=
NM_001318905.1:c.969G>A	NP_001305834.1:p.Thr323=
NM_001318906.1:c.969G>A	NP_001305835.1:p.Thr323=
NM_005271.4:c.1470G>A	NP_005262.1:p.Thr490=
NM_005271.5:c.1470G>A MANE Select	NP_005262.1:p.Thr490=
NM_001318904.2:c.969G>A	NP_001305833.1:p.Thr323=
NM_001318905.2:c.969G>A	NP_001305834.1:p.Thr323=
NM_001318906.2:c.969G>A	NP_001305835.1:p.Thr323=