Canonical Allele Identifier: CA1165412716

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930586C= , CM000663.2:g.42930586C=	GRCh38
NC_000001.10:g.43396257C= , CM000663.1:g.43396257C=	GRCh37
NC_000001.9:g.43168844C=	NCBI36
NG_008232.1:g.33591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.516+40G= MANE Select	ENSP00000416293.2:n.516+40G=
ENST00000674765.1:c.516+40G=	ENSP00000501811.1:n.516+40G=
ENST00000675112.1:n.539+40G=
ENST00000676254.1:n.965+40G=
ENST00000426263.7:c.516+40G=	ENSP00000416293.2:n.516+40G=
ENST00000439722.2:c.395+40G=	ENSP00000395521.2:n.395+40G=
ENST00000475162.3:c.415+40G=
ENST00000625233.2:n.764G=
ENST00000630287.2:c.516+40G=	ENSP00000486694.1:n.516+40G=
NM_006516.2:c.516+40G=	NP_006507.2:n.516+40G=
NM_006516.3:c.516+40G=	NP_006507.2:n.516+40G=
NM_006516.4:c.516+40G= MANE Select	NP_006507.2:n.516+40G=