Canonical Allele Identifier: CA2702479

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170999071C>T , CM000665.2:g.170999071C>T	GRCh38
NC_000003.11:g.170716860C>T , CM000665.1:g.170716860C>T	GRCh37
NC_000003.10:g.172199554C>T	NCBI36
NG_008108.1:g.32909G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.1164G>A MANE Select	NP_000331.1:p.Val388=
ENST00000314251.8:c.1164G>A MANE Select	ENSP00000323568.3:p.Val388=
NM_000340.1:c.1164G>A	NP_000331.1:p.Val388=
NM_001278658.1:c.807G>A	NP_001265587.1:p.Val269=
NM_001278658.2:c.807G>A	NP_001265587.1:p.Val269=
NM_001278659.1:c.645G>A	NP_001265588.1:p.Val215=
NM_001278659.2:c.645G>A	NP_001265588.1:p.Val215=
ENST00000314251.7:c.1164G>A	ENSP00000323568.3:p.Val388=
ENST00000469787.1:c.*631G>A	ENSP00000417918.1:n.*631G>A
ENST00000497642.5:c.*631G>A	ENSP00000418456.1:n.*631G>A
XM_011513087.1:c.1119G>A	XP_011511389.1:p.Val373=
XM_011513087.2:c.1119G>A	XP_011511389.1:p.Val373=
XM_011513088.1:c.945G>A	XP_011511390.1:p.Val315=
XM_011513089.1:c.645G>A	XP_011511391.1:p.Val215=
XM_024453720.1:c.645G>A	XP_024309488.1:p.Val215=