Canonical Allele Identifier: CA2702507

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171002575C>T , CM000665.2:g.171002575C>T	GRCh38
NC_000003.11:g.170720364C>T , CM000665.1:g.170720364C>T	GRCh37
NC_000003.10:g.172203058C>T	NCBI36
NG_008108.1:g.29405G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.1068+1G>A MANE Select	ENSP00000323568.3:n.1068+1G>A
ENST00000314251.7:c.1068+1G>A	ENSP00000323568.3:n.1068+1G>A
ENST00000469787.1:c.*535+1G>A	ENSP00000417918.1:n.*535+1G>A
ENST00000497642.5:c.*535+1G>A	ENSP00000418456.1:n.*535+1G>A
NM_000340.1:c.1068+1G>A	NP_000331.1:n.1068+1G>A
NM_001278658.1:c.711+1G>A	NP_001265587.1:n.711+1G>A
NM_001278659.1:c.549+1G>A	NP_001265588.1:n.549+1G>A
XM_011513087.1:c.1023+1G>A	XP_011511389.1:n.1023+1G>A
XM_011513088.1:c.849+1G>A	XP_011511390.1:n.849+1G>A
XM_011513089.1:c.549+1G>A	XP_011511391.1:n.549+1G>A
XM_011513087.2:c.1023+1G>A	XP_011511389.1:n.1023+1G>A
XM_024453720.1:c.549+1G>A	XP_024309488.1:n.549+1G>A
NM_000340.2:c.1068+1G>A MANE Select	NP_000331.1:n.1068+1G>A
NM_001278658.2:c.711+1G>A	NP_001265587.1:n.711+1G>A
NM_001278659.2:c.549+1G>A	NP_001265588.1:n.549+1G>A