Canonical Allele Identifier: CA1165412775

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930731T= , CM000663.2:g.42930731T=	GRCh38
NC_000001.10:g.43396402T= , CM000663.1:g.43396402T=	GRCh37
NC_000001.9:g.43168989T=	NCBI36
NG_008232.1:g.33446A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.411A= MANE Select	ENSP00000416293.2:p.Thr137=
ENST00000674765.1:c.411A=	ENSP00000501811.1:p.Thr137=
ENST00000675112.1:n.434A=
ENST00000676254.1:n.860A=
ENST00000372500.4:c.315A=	ENSP00000361578.4:p.Thr105=
ENST00000426263.7:c.411A=	ENSP00000416293.2:p.Thr137=
ENST00000439722.2:c.290A=	ENSP00000395521.2:n.290A=
ENST00000475162.3:c.310A=
ENST00000625233.2:n.619A=
ENST00000630287.2:c.411A=	ENSP00000486694.1:p.Thr137=
NM_006516.2:c.411A=	NP_006507.2:p.Thr137=
NM_006516.3:c.411A=	NP_006507.2:p.Thr137=
NM_006516.4:c.411A= MANE Select	NP_006507.2:p.Thr137=