Canonical Allele Identifier: CA2610017616

Gene: GLUD1

Linked Data

• gnomAD v4: 10-87051659-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87051659A>G , CM000672.2:g.87051659A>G	GRCh38
NC_000010.10:g.88811416A>G , CM000672.1:g.88811416A>G	GRCh37
NC_000010.9:g.88801396A>G	NCBI36
NG_013010.1:g.48361T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474574.2:n.3344T>C
ENST00000487058.2:n.1516T>C
ENST00000681987.1:n.1607T>C
ENST00000681988.1:c.*92T>C	ENSP00000507316.1:n.*92T>C
ENST00000682396.1:c.1760T>C	ENSP00000506764.1:n.1760T>C
ENST00000682507.1:c.*92T>C	ENSP00000508098.1:n.*92T>C
ENST00000682622.1:c.2049T>C	ENSP00000506732.1:n.2049T>C
ENST00000682833.1:c.1604T>C
ENST00000683022.1:c.1790T>C
ENST00000683256.1:c.*92T>C	ENSP00000507901.1:n.*92T>C
ENST00000683269.1:c.*92T>C	ENSP00000508107.1:n.*92T>C
ENST00000683647.1:n.5103T>C
ENST00000683649.1:n.619T>C
ENST00000683783.1:c.*92T>C	ENSP00000507881.1:n.*92T>C
ENST00000683813.1:n.1497T>C
ENST00000684032.1:c.1624T>C	ENSP00000506969.1:n.1624T>C
ENST00000684201.1:c.*92T>C	ENSP00000507887.1:n.*92T>C
ENST00000684338.1:c.1847T>C	ENSP00000507457.1:n.1847T>C
ENST00000684372.1:c.*92T>C	ENSP00000508244.1:n.*92T>C
ENST00000684434.1:c.1240T>C
ENST00000684546.1:c.*92T>C	ENSP00000507729.1:n.*92T>C
ENST00000684665.1:n.733T>C
ENST00000684690.1:n.1996T>C
ENST00000684699.1:n.4348T>C
ENST00000277865.5:c.*92T>C MANE Select	ENSP00000277865.4:n.*92T>C
ENST00000277865.4:c.*92T>C	ENSP00000277865.4:n.*92T>C
NM_005271.3:c.*92T>C	NP_005262.1:n.*92T>C
XM_011539668.1:c.*92T>C	XP_011537970.1:n.*92T>C
XM_011539669.1:c.*92T>C	XP_011537971.1:n.*92T>C
NM_001318900.1:c.*92T>C	NP_001305829.1:n.*92T>C
NM_001318901.1:c.*92T>C	NP_001305830.1:n.*92T>C
NM_001318902.1:c.*92T>C	NP_001305831.1:n.*92T>C
NM_001318904.1:c.*92T>C	NP_001305833.1:n.*92T>C
NM_001318905.1:c.*92T>C	NP_001305834.1:n.*92T>C
NM_001318906.1:c.*92T>C	NP_001305835.1:n.*92T>C
NM_005271.4:c.*92T>C	NP_005262.1:n.*92T>C
NM_005271.5:c.*92T>C MANE Select	NP_005262.1:n.*92T>C
NM_001318904.2:c.*92T>C	NP_001305833.1:n.*92T>C
NM_001318905.2:c.*92T>C	NP_001305834.1:n.*92T>C
NM_001318906.2:c.*92T>C	NP_001305835.1:n.*92T>C