Canonical Allele Identifier: CA1925786984

Gene: GLUD1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87050495A= , CM000672.2:g.87050495A=	GRCh38
NC_000010.10:g.88810252A= , CM000672.1:g.88810252A=	GRCh37
NC_000010.9:g.88800232A=	NCBI36
NG_013010.1:g.49525T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684699.1:n.5512T=
ENST00000277865.5:c.*1256T= MANE Select	ENSP00000277865.4:n.*1256T=
ENST00000277865.4:c.*1256T=	ENSP00000277865.4:n.*1256T=
NM_005271.3:c.*1256T=	NP_005262.1:n.*1256T=
XM_011539668.1:c.*1256T=	XP_011537970.1:n.*1256T=
XM_011539669.1:c.*1256T=	XP_011537971.1:n.*1256T=
NM_001318900.1:c.*1256T=	NP_001305829.1:n.*1256T=
NM_001318901.1:c.*1256T=	NP_001305830.1:n.*1256T=
NM_001318902.1:c.*1256T=	NP_001305831.1:n.*1256T=
NM_001318904.1:c.*1256T=	NP_001305833.1:n.*1256T=
NM_001318905.1:c.*1256T=	NP_001305834.1:n.*1256T=
NM_001318906.1:c.*1256T=	NP_001305835.1:n.*1256T=
NM_005271.4:c.*1256T=	NP_005262.1:n.*1256T=
NM_005271.5:c.*1256T= MANE Select	NP_005262.1:n.*1256T=
NM_001318904.2:c.*1256T=	NP_001305833.1:n.*1256T=
NM_001318905.2:c.*1256T=	NP_001305834.1:n.*1256T=
NM_001318906.2:c.*1256T=	NP_001305835.1:n.*1256T=