Canonical Allele Identifier: CA355490798

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007265T>C , CM000665.2:g.171007265T>C	GRCh38
NC_000003.11:g.170725054T>C , CM000665.1:g.170725054T>C	GRCh37
NC_000003.10:g.172207748T>C	NCBI36
NG_008108.1:g.24715A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.497-2A>G MANE Select	NP_000331.1:n.497-2A>G
ENST00000314251.8:c.497-2A>G MANE Select	ENSP00000323568.3:n.497-2A>G
NM_000340.1:c.497-2A>G	NP_000331.1:n.497-2A>G
NM_001278658.1:c.140-2A>G	NP_001265587.1:n.140-2A>G
NM_001278658.2:c.140-2A>G	NP_001265587.1:n.140-2A>G
NM_001278659.1:c.-23-2A>G	NP_001265588.1:n.-23-2A>G
NM_001278659.2:c.-23-2A>G	NP_001265588.1:n.-23-2A>G
ENST00000314251.7:c.497-2A>G	ENSP00000323568.3:n.497-2A>G
ENST00000461867.1:c.-23-2A>G	ENSP00000418888.1:n.-23-2A>G
ENST00000469787.1:c.234-2A>G	ENSP00000417918.1:n.234-2A>G
ENST00000471379.1:n.206A>G
ENST00000497642.5:c.372-2A>G	ENSP00000418456.1:n.372-2A>G
XM_011513087.1:c.452-2A>G	XP_011511389.1:n.452-2A>G
XM_011513087.2:c.452-2A>G	XP_011511389.1:n.452-2A>G
XM_011513088.1:c.278-2A>G	XP_011511390.1:n.278-2A>G
XM_011513089.1:c.-23-2A>G	XP_011511391.1:n.-23-2A>G
XM_024453720.1:c.-23-2A>G	XP_024309488.1:n.-23-2A>G