Canonical Allele Identifier: CA355492561

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171014489C>T , CM000665.2:g.171014489C>T	GRCh38
NC_000003.11:g.170732278C>T , CM000665.1:g.170732278C>T	GRCh37
NC_000003.10:g.172214972C>T	NCBI36
NG_008108.1:g.17491G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.351G>A MANE Select	NP_000331.1:p.Trp117Ter
ENST00000314251.8:c.351G>A MANE Select	ENSP00000323568.3:p.Trp117Ter
NM_000340.1:c.351G>A	NP_000331.1:p.Trp117Ter
NM_001278658.1:c.14+4042G>A	NP_001265587.1:n.14+4042G>A
NM_001278658.2:c.14+4042G>A	NP_001265587.1:n.14+4042G>A
NM_001278659.1:c.-44G>A	NP_001265588.1:n.-44G>A
NM_001278659.2:c.-44G>A	NP_001265588.1:n.-44G>A
ENST00000314251.7:c.351G>A	ENSP00000323568.3:p.Trp117Ter
ENST00000461867.1:c.-24+4042G>A	ENSP00000418888.1:n.-24+4042G>A
ENST00000469787.1:c.108+4042G>A	ENSP00000417918.1:n.108+4042G>A
ENST00000497642.5:c.351G>A	ENSP00000418456.1:p.Trp117Ter
XM_011513087.1:c.306G>A	XP_011511389.1:p.Trp102Ter
XM_011513087.2:c.306G>A	XP_011511389.1:p.Trp102Ter
XM_011513088.1:c.132G>A	XP_011511390.1:p.Trp44Ter
XM_011513089.1:c.-24+4042G>A	XP_011511391.1:n.-24+4042G>A
XM_024453720.1:c.-24+4042G>A	XP_024309488.1:n.-24+4042G>A