Canonical Allele Identifier: CA355491527

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171009956A>T , CM000665.2:g.171009956A>T	GRCh38
NC_000003.11:g.170727745A>T , CM000665.1:g.170727745A>T	GRCh37
NC_000003.10:g.172210439A>T	NCBI36
NG_008108.1:g.22024T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.496+2T>A MANE Select	NP_000331.1:n.496+2T>A
ENST00000314251.8:c.496+2T>A MANE Select	ENSP00000323568.3:n.496+2T>A
NM_000340.1:c.496+2T>A	NP_000331.1:n.496+2T>A
NM_001278658.1:c.139+2T>A	NP_001265587.1:n.139+2T>A
NM_001278658.2:c.139+2T>A	NP_001265587.1:n.139+2T>A
NM_001278659.1:c.-23-2693T>A	NP_001265588.1:n.-23-2693T>A
NM_001278659.2:c.-23-2693T>A	NP_001265588.1:n.-23-2693T>A
ENST00000314251.7:c.496+2T>A	ENSP00000323568.3:n.496+2T>A
ENST00000461867.1:c.-23-2693T>A	ENSP00000418888.1:n.-23-2693T>A
ENST00000469787.1:c.233+2T>A	ENSP00000417918.1:n.233+2T>A
ENST00000497642.5:c.372-2693T>A	ENSP00000418456.1:n.372-2693T>A
XM_011513087.1:c.451+2T>A	XP_011511389.1:n.451+2T>A
XM_011513087.2:c.451+2T>A	XP_011511389.1:n.451+2T>A
XM_011513088.1:c.277+2T>A	XP_011511390.1:n.277+2T>A
XM_011513089.1:c.-23-2693T>A	XP_011511391.1:n.-23-2693T>A
XM_024453720.1:c.-23-2693T>A	XP_024309488.1:n.-23-2693T>A