Canonical Allele Identifier: CA020026

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007166C>T , CM000665.2:g.171007166C>T	GRCh38
NC_000003.11:g.170724955C>T , CM000665.1:g.170724955C>T	GRCh37
NC_000003.10:g.172207649C>T	NCBI36
NG_008108.1:g.24814G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.594G>A MANE Select	ENSP00000323568.3:p.Thr198=
ENST00000314251.7:c.594G>A	ENSP00000323568.3:p.Thr198=
ENST00000461867.1:c.75G>A	ENSP00000418888.1:p.Thr25=
ENST00000469787.1:c.*61G>A	ENSP00000417918.1:n.*61G>A
ENST00000471379.1:n.305G>A
ENST00000497642.5:c.*61G>A	ENSP00000418456.1:n.*61G>A
NM_000340.1:c.594G>A	NP_000331.1:p.Thr198=
NM_001278658.1:c.237G>A	NP_001265587.1:p.Thr79=
NM_001278659.1:c.75G>A	NP_001265588.1:p.Thr25=
XM_011513087.1:c.549G>A	XP_011511389.1:p.Thr183=
XM_011513088.1:c.375G>A	XP_011511390.1:p.Thr125=
XM_011513089.1:c.75G>A	XP_011511391.1:p.Thr25=
XM_011513087.2:c.549G>A	XP_011511389.1:p.Thr183=
XM_024453720.1:c.75G>A	XP_024309488.1:p.Thr25=
NM_000340.2:c.594G>A MANE Select	NP_000331.1:p.Thr198=
NM_001278658.2:c.237G>A	NP_001265587.1:p.Thr79=
NM_001278659.2:c.75G>A	NP_001265588.1:p.Thr25=