Canonical Allele Identifier: CA1165417705

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943073A= , CM000663.2:g.42943073A=	GRCh38
NC_000001.10:g.43408744A= , CM000663.1:g.43408744A=	GRCh37
NC_000001.9:g.43181331A=	NCBI36
NG_008232.1:g.21104T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.114+153T= MANE Select	ENSP00000416293.2:n.114+153T=
ENST00000674765.1:c.114+153T=	ENSP00000501811.1:n.114+153T=
ENST00000675112.1:n.137+153T=
ENST00000372500.4:c.19-11867T=	ENSP00000361578.4:n.19-11867T=
ENST00000415851.6:n.331+153T=
ENST00000426263.7:c.114+153T=	ENSP00000416293.2:n.114+153T=
ENST00000475162.3:c.13+153T=
ENST00000625233.2:n.322+153T=
ENST00000628173.1:n.333+153T=
ENST00000630287.2:c.114+153T=	ENSP00000486694.1:n.114+153T=
ENST00000630821.1:n.484T=
NM_006516.2:c.114+153T=	NP_006507.2:n.114+153T=
NM_006516.3:c.114+153T=	NP_006507.2:n.114+153T=
NM_006516.4:c.114+153T= MANE Select	NP_006507.2:n.114+153T=