Canonical Allele Identifier: CA377466929

Gene: GLUD1

Linked Data

• gnomAD v4: 10-87060740-G-A
• MyVariant Identifiers: chr10:g.88820497G>A (hg19) ; chr10:g.87060740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87060740G>A , CM000672.2:g.87060740G>A	GRCh38
NC_000010.10:g.88820497G>A , CM000672.1:g.88820497G>A	GRCh37
NC_000010.9:g.88810477G>A	NCBI36
NG_013010.1:g.39280C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474574.2:n.2720C>T
ENST00000487058.2:n.446C>T
ENST00000681987.1:n.983C>T
ENST00000681988.1:c.644C>T	ENSP00000507316.1:p.Ala215Val
ENST00000682396.1:c.1136C>T	ENSP00000506764.1:n.1136C>T
ENST00000682507.1:c.644C>T	ENSP00000508098.1:p.Ala215Val
ENST00000682622.1:c.1425C>T	ENSP00000506732.1:n.1425C>T
ENST00000682833.1:c.980C>T
ENST00000683022.1:c.1166C>T
ENST00000683256.1:c.644C>T	ENSP00000507901.1:p.Ala215Val
ENST00000683269.1:c.644C>T	ENSP00000508107.1:p.Ala215Val
ENST00000683647.1:n.4479C>T
ENST00000683783.1:c.644C>T	ENSP00000507881.1:p.Ala215Val
ENST00000683813.1:n.873C>T
ENST00000684032.1:c.1000C>T	ENSP00000506969.1:n.1000C>T
ENST00000684201.1:c.922-499C>T	ENSP00000507887.1:n.922-499C>T
ENST00000684338.1:c.1145C>T	ENSP00000507457.1:p.Ala382Val
ENST00000684372.1:c.644C>T	ENSP00000508244.1:p.Ala215Val
ENST00000684392.1:n.1876C>T
ENST00000684434.1:c.616C>T
ENST00000684546.1:c.644C>T	ENSP00000507729.1:p.Ala215Val
ENST00000684690.1:n.926C>T
ENST00000684699.1:n.3278C>T
ENST00000277865.5:c.1145C>T MANE Select	ENSP00000277865.4:p.Ala382Val
ENST00000277865.4:c.1145C>T	ENSP00000277865.4:p.Ala382Val
ENST00000465164.1:n.224C>T
NM_005271.3:c.1145C>T	NP_005262.1:p.Ala382Val
XM_011539668.1:c.644C>T	XP_011537970.1:p.Ala215Val
XM_011539669.1:c.644C>T	XP_011537971.1:p.Ala215Val
NM_001318900.1:c.746C>T	NP_001305829.1:p.Ala249Val
NM_001318901.1:c.644C>T	NP_001305830.1:p.Ala215Val
NM_001318902.1:c.644C>T	NP_001305831.1:p.Ala215Val
NM_001318904.1:c.644C>T	NP_001305833.1:p.Ala215Val
NM_001318905.1:c.644C>T	NP_001305834.1:p.Ala215Val
NM_001318906.1:c.644C>T	NP_001305835.1:p.Ala215Val
NM_005271.4:c.1145C>T	NP_005262.1:p.Ala382Val
NM_005271.5:c.1145C>T MANE Select	NP_005262.1:p.Ala382Val
NM_001318904.2:c.644C>T	NP_001305833.1:p.Ala215Val
NM_001318905.2:c.644C>T	NP_001305834.1:p.Ala215Val
NM_001318906.2:c.644C>T	NP_001305835.1:p.Ala215Val