Canonical Allele Identifier: CA355492654

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171014512T>A , CM000665.2:g.171014512T>A	GRCh38
NC_000003.11:g.170732301T>A , CM000665.1:g.170732301T>A	GRCh37
NC_000003.10:g.172214995T>A	NCBI36
NG_008108.1:g.17468A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.328A>T MANE Select	NP_000331.1:p.Thr110Ser
ENST00000314251.8:c.328A>T MANE Select	ENSP00000323568.3:p.Thr110Ser
NM_000340.1:c.328A>T	NP_000331.1:p.Thr110Ser
NM_001278658.1:c.14+4019A>T	NP_001265587.1:n.14+4019A>T
NM_001278658.2:c.14+4019A>T	NP_001265587.1:n.14+4019A>T
NM_001278659.1:c.-67A>T	NP_001265588.1:n.-67A>T
NM_001278659.2:c.-67A>T	NP_001265588.1:n.-67A>T
ENST00000314251.7:c.328A>T	ENSP00000323568.3:p.Thr110Ser
ENST00000461867.1:c.-24+4019A>T	ENSP00000418888.1:n.-24+4019A>T
ENST00000469787.1:c.108+4019A>T	ENSP00000417918.1:n.108+4019A>T
ENST00000497642.5:c.328A>T	ENSP00000418456.1:p.Thr110Ser
XM_011513087.1:c.283A>T	XP_011511389.1:p.Thr95Ser
XM_011513087.2:c.283A>T	XP_011511389.1:p.Thr95Ser
XM_011513088.1:c.109A>T	XP_011511390.1:p.Thr37Ser
XM_011513089.1:c.-24+4019A>T	XP_011511391.1:n.-24+4019A>T
XM_024453720.1:c.-24+4019A>T	XP_024309488.1:n.-24+4019A>T