Canonical Allele Identifier: CA1420165485

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007013A= , CM000665.2:g.171007013A=	GRCh38
NC_000003.11:g.170724802A= , CM000665.1:g.170724802A=	GRCh37
NC_000003.10:g.172207496A=	NCBI36
NG_008108.1:g.24967T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.612+135T= MANE Select	ENSP00000323568.3:n.612+135T=
ENST00000314251.7:c.612+135T=	ENSP00000323568.3:n.612+135T=
ENST00000461867.1:c.93+135T=	ENSP00000418888.1:n.93+135T=
ENST00000469787.1:c.*79+135T=	ENSP00000417918.1:n.*79+135T=
ENST00000471379.1:n.323+135T=
ENST00000497642.5:c.*79+135T=	ENSP00000418456.1:n.*79+135T=
NM_000340.1:c.612+135T=	NP_000331.1:n.612+135T=
NM_001278658.1:c.255+135T=	NP_001265587.1:n.255+135T=
NM_001278659.1:c.93+135T=	NP_001265588.1:n.93+135T=
XM_011513087.1:c.567+135T=	XP_011511389.1:n.567+135T=
XM_011513088.1:c.393+135T=	XP_011511390.1:n.393+135T=
XM_011513089.1:c.93+135T=	XP_011511391.1:n.93+135T=
XM_011513087.2:c.567+135T=	XP_011511389.1:n.567+135T=
XM_024453720.1:c.93+135T=	XP_024309488.1:n.93+135T=
NM_000340.2:c.612+135T= MANE Select	NP_000331.1:n.612+135T=
NM_001278658.2:c.255+135T=	NP_001265587.1:n.255+135T=
NM_001278659.2:c.93+135T=	NP_001265588.1:n.93+135T=