Canonical Allele Identifier: CA355486202

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170999064C>A , CM000665.2:g.170999064C>A	GRCh38
NC_000003.11:g.170716853C>A , CM000665.1:g.170716853C>A	GRCh37
NC_000003.10:g.172199547C>A	NCBI36
NG_008108.1:g.32916G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.1170+1G>T MANE Select	NP_000331.1:n.1170+1G>T
ENST00000314251.8:c.1170+1G>T MANE Select	ENSP00000323568.3:n.1170+1G>T
NM_000340.1:c.1170+1G>T	NP_000331.1:n.1170+1G>T
NM_001278658.1:c.813+1G>T	NP_001265587.1:n.813+1G>T
NM_001278658.2:c.813+1G>T	NP_001265587.1:n.813+1G>T
NM_001278659.1:c.651+1G>T	NP_001265588.1:n.651+1G>T
NM_001278659.2:c.651+1G>T	NP_001265588.1:n.651+1G>T
ENST00000314251.7:c.1170+1G>T	ENSP00000323568.3:n.1170+1G>T
ENST00000469787.1:c.*637+1G>T	ENSP00000417918.1:n.*637+1G>T
ENST00000497642.5:c.*637+1G>T	ENSP00000418456.1:n.*637+1G>T
XM_011513087.1:c.1125+1G>T	XP_011511389.1:n.1125+1G>T
XM_011513087.2:c.1125+1G>T	XP_011511389.1:n.1125+1G>T
XM_011513088.1:c.951+1G>T	XP_011511390.1:n.951+1G>T
XM_011513089.1:c.651+1G>T	XP_011511391.1:n.651+1G>T
XM_024453720.1:c.651+1G>T	XP_024309488.1:n.651+1G>T