Canonical Allele Identifier: CA1420168487

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171014426A= , CM000665.2:g.171014426A=	GRCh38
NC_000003.11:g.170732215A= , CM000665.1:g.170732215A=	GRCh37
NC_000003.10:g.172214909A=	NCBI36
NG_008108.1:g.17554T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.371+43T= MANE Select	ENSP00000323568.3:n.371+43T=
ENST00000314251.7:c.371+43T=	ENSP00000323568.3:n.371+43T=
ENST00000461867.1:c.-24+4105T=	ENSP00000418888.1:n.-24+4105T=
ENST00000469787.1:c.108+4105T=	ENSP00000417918.1:n.108+4105T=
ENST00000497642.5:c.371+43T=	ENSP00000418456.1:n.371+43T=
NM_000340.1:c.371+43T=	NP_000331.1:n.371+43T=
NM_001278658.1:c.14+4105T=	NP_001265587.1:n.14+4105T=
NM_001278659.1:c.-24+43T=	NP_001265588.1:n.-24+43T=
XM_011513087.1:c.326+43T=	XP_011511389.1:n.326+43T=
XM_011513088.1:c.152+43T=	XP_011511390.1:n.152+43T=
XM_011513089.1:c.-24+4105T=	XP_011511391.1:n.-24+4105T=
XM_011513087.2:c.326+43T=	XP_011511389.1:n.326+43T=
XM_024453720.1:c.-24+4105T=	XP_024309488.1:n.-24+4105T=
NM_000340.2:c.371+43T= MANE Select	NP_000331.1:n.371+43T=
NM_001278658.2:c.14+4105T=	NP_001265587.1:n.14+4105T=
NM_001278659.2:c.-24+43T=	NP_001265588.1:n.-24+43T=