Canonical Allele Identifier: CA1149065438

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943473A= , CM000663.2:g.42943473A=	GRCh38
NC_000001.10:g.43409144A= , CM000663.1:g.43409144A=	GRCh37
NC_000001.9:g.43181731A=	NCBI36
NG_008232.1:g.20704T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.19-152T= MANE Select	ENSP00000416293.2:n.19-152T=
ENST00000674765.1:c.19-152T=	ENSP00000501811.1:n.19-152T=
ENST00000675112.1:n.42-152T=
ENST00000372500.4:c.19-12267T=	ENSP00000361578.4:n.19-12267T=
ENST00000415851.6:n.236-152T=
ENST00000426263.7:c.19-152T=	ENSP00000416293.2:n.19-152T=
ENST00000625233.2:n.227-152T=
ENST00000628173.1:n.238-152T=
ENST00000630287.2:c.19-152T=	ENSP00000486694.1:n.19-152T=
ENST00000630821.1:n.236-152T=
NM_006516.2:c.19-152T=	NP_006507.2:n.19-152T=
NM_006516.3:c.19-152T=	NP_006507.2:n.19-152T=
NM_006516.4:c.19-152T= MANE Select	NP_006507.2:n.19-152T=