Canonical Allele Identifier: CA470666604

Gene: GLUD1

Linked Data

• MyVariant Identifiers: chr10:g.88813153A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87053396A>T , CM000672.2:g.87053396A>T	GRCh38
NC_000010.10:g.88813153A>T , CM000672.1:g.88813153A>T	GRCh37
NC_000010.9:g.88803133A>T	NCBI36
NG_013010.1:g.46624T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474574.2:n.3078T>A
ENST00000487058.2:n.1250T>A
ENST00000681987.1:n.1341T>A
ENST00000681988.1:c.1002T>A	ENSP00000507316.1:p.Ser334=
ENST00000682396.1:c.1494T>A	ENSP00000506764.1:n.1494T>A
ENST00000682507.1:c.1002T>A	ENSP00000508098.1:p.Ser334=
ENST00000682622.1:c.1783T>A	ENSP00000506732.1:n.1783T>A
ENST00000682833.1:c.1338T>A
ENST00000683022.1:c.1524T>A
ENST00000683256.1:c.1002T>A	ENSP00000507901.1:p.Ser334=
ENST00000683269.1:c.1002T>A	ENSP00000508107.1:p.Ser334=
ENST00000683647.1:n.4837T>A
ENST00000683649.1:n.353T>A
ENST00000683783.1:c.1002T>A	ENSP00000507881.1:p.Ser334=
ENST00000683813.1:n.1231T>A
ENST00000684032.1:c.1358T>A	ENSP00000506969.1:n.1358T>A
ENST00000684201.1:c.1227T>A	ENSP00000507887.1:p.Ser409=
ENST00000684338.1:c.1503T>A	ENSP00000507457.1:p.Ser501=
ENST00000684372.1:c.1002T>A	ENSP00000508244.1:p.Ser334=
ENST00000684434.1:c.974T>A
ENST00000684546.1:c.1002T>A	ENSP00000507729.1:p.Ser334=
ENST00000684665.1:n.467T>A
ENST00000684690.1:n.1730T>A
ENST00000684699.1:n.4082T>A
ENST00000277865.5:c.1503T>A MANE Select	ENSP00000277865.4:p.Ser501=
ENST00000277865.4:c.1503T>A	ENSP00000277865.4:p.Ser501=
NM_005271.3:c.1503T>A	NP_005262.1:p.Ser501=
XM_011539668.1:c.1002T>A	XP_011537970.1:p.Ser334=
XM_011539669.1:c.1002T>A	XP_011537971.1:p.Ser334=
NM_001318900.1:c.1104T>A	NP_001305829.1:p.Ser368=
NM_001318901.1:c.1002T>A	NP_001305830.1:p.Ser334=
NM_001318902.1:c.1002T>A	NP_001305831.1:p.Ser334=
NM_001318904.1:c.1002T>A	NP_001305833.1:p.Ser334=
NM_001318905.1:c.1002T>A	NP_001305834.1:p.Ser334=
NM_001318906.1:c.1002T>A	NP_001305835.1:p.Ser334=
NM_005271.4:c.1503T>A	NP_005262.1:p.Ser501=
NM_005271.5:c.1503T>A MANE Select	NP_005262.1:p.Ser501=
NM_001318904.2:c.1002T>A	NP_001305833.1:p.Ser334=
NM_001318905.2:c.1002T>A	NP_001305834.1:p.Ser334=
NM_001318906.2:c.1002T>A	NP_001305835.1:p.Ser334=