Canonical Allele Identifier: CA377467179

Gene: GLUD1

Linked Data

• MyVariant Identifiers: chr10:g.88820671C>A (hg19) ; chr10:g.87060914C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87060914C>A , CM000672.2:g.87060914C>A	GRCh38
NC_000010.10:g.88820671C>A , CM000672.1:g.88820671C>A	GRCh37
NC_000010.9:g.88810651C>A	NCBI36
NG_013010.1:g.39106G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474574.2:n.2634+1G>T
ENST00000487058.2:n.272G>T
ENST00000681987.1:n.897+1G>T
ENST00000681988.1:c.558+1G>T	ENSP00000507316.1:n.558+1G>T
ENST00000682396.1:c.1050+1G>T	ENSP00000506764.1:n.1050+1G>T
ENST00000682507.1:c.558+1G>T	ENSP00000508098.1:n.558+1G>T
ENST00000682622.1:c.1339+1G>T	ENSP00000506732.1:n.1339+1G>T
ENST00000682833.1:c.894+1G>T
ENST00000683022.1:c.1080+1G>T
ENST00000683256.1:c.558+1G>T	ENSP00000507901.1:n.558+1G>T
ENST00000683269.1:c.558+1G>T	ENSP00000508107.1:n.558+1G>T
ENST00000683647.1:n.4393+1G>T
ENST00000683783.1:c.558+1G>T	ENSP00000507881.1:n.558+1G>T
ENST00000683813.1:n.787+1G>T
ENST00000684032.1:c.914+1G>T	ENSP00000506969.1:n.914+1G>T
ENST00000684201.1:c.922-673G>T	ENSP00000507887.1:n.922-673G>T
ENST00000684338.1:c.1059+1G>T	ENSP00000507457.1:n.1059+1G>T
ENST00000684372.1:c.558+1G>T	ENSP00000508244.1:n.558+1G>T
ENST00000684392.1:n.1790+1G>T
ENST00000684434.1:c.530+1G>T
ENST00000684546.1:c.558+1G>T	ENSP00000507729.1:n.558+1G>T
ENST00000684690.1:n.840+1G>T
ENST00000684699.1:n.3192+1G>T
ENST00000277865.5:c.1059+1G>T MANE Select	ENSP00000277865.4:n.1059+1G>T
ENST00000277865.4:c.1059+1G>T	ENSP00000277865.4:n.1059+1G>T
ENST00000465164.1:n.138+1G>T
NM_005271.3:c.1059+1G>T	NP_005262.1:n.1059+1G>T
XM_011539668.1:c.558+1G>T	XP_011537970.1:n.558+1G>T
XM_011539669.1:c.558+1G>T	XP_011537971.1:n.558+1G>T
NM_001318900.1:c.660+1G>T	NP_001305829.1:n.660+1G>T
NM_001318901.1:c.558+1G>T	NP_001305830.1:n.558+1G>T
NM_001318902.1:c.558+1G>T	NP_001305831.1:n.558+1G>T
NM_001318904.1:c.558+1G>T	NP_001305833.1:n.558+1G>T
NM_001318905.1:c.558+1G>T	NP_001305834.1:n.558+1G>T
NM_001318906.1:c.558+1G>T	NP_001305835.1:n.558+1G>T
NM_005271.4:c.1059+1G>T	NP_005262.1:n.1059+1G>T
NM_005271.5:c.1059+1G>T MANE Select	NP_005262.1:n.1059+1G>T
NM_001318904.2:c.558+1G>T	NP_001305833.1:n.558+1G>T
NM_001318905.2:c.558+1G>T	NP_001305834.1:n.558+1G>T
NM_001318906.2:c.558+1G>T	NP_001305835.1:n.558+1G>T