Canonical Allele Identifier: CA2702635

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007167G>A , CM000665.2:g.171007167G>A	GRCh38
NC_000003.11:g.170724956G>A , CM000665.1:g.170724956G>A	GRCh37
NC_000003.10:g.172207650G>A	NCBI36
NG_008108.1:g.24813C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.593C>T MANE Select	NP_000331.1:p.Thr198Met
ENST00000314251.8:c.593C>T MANE Select	ENSP00000323568.3:p.Thr198Met
NM_000340.1:c.593C>T	NP_000331.1:p.Thr198Met
NM_001278658.1:c.236C>T	NP_001265587.1:p.Thr79Met
NM_001278658.2:c.236C>T	NP_001265587.1:p.Thr79Met
NM_001278659.1:c.74C>T	NP_001265588.1:p.Thr25Met
NM_001278659.2:c.74C>T	NP_001265588.1:p.Thr25Met
ENST00000314251.7:c.593C>T	ENSP00000323568.3:p.Thr198Met
ENST00000461867.1:c.74C>T	ENSP00000418888.1:p.Thr25Met
ENST00000469787.1:c.*60C>T	ENSP00000417918.1:n.*60C>T
ENST00000471379.1:n.304C>T
ENST00000497642.5:c.*60C>T	ENSP00000418456.1:n.*60C>T
XM_011513087.1:c.548C>T	XP_011511389.1:p.Thr183Met
XM_011513087.2:c.548C>T	XP_011511389.1:p.Thr183Met
XM_011513088.1:c.374C>T	XP_011511390.1:p.Thr125Met
XM_011513089.1:c.74C>T	XP_011511391.1:p.Thr25Met
XM_024453720.1:c.74C>T	XP_024309488.1:p.Thr25Met