Canonical Allele Identifier: CA1420165562

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007173A= , CM000665.2:g.171007173A=	GRCh38
NC_000003.11:g.170724962A= , CM000665.1:g.170724962A=	GRCh37
NC_000003.10:g.172207656A=	NCBI36
NG_008108.1:g.24807T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.587T= MANE Select	ENSP00000323568.3:p.Ile196=
ENST00000314251.7:c.587T=	ENSP00000323568.3:p.Ile196=
ENST00000461867.1:c.68T=	ENSP00000418888.1:p.Ile23=
ENST00000469787.1:c.*54T=	ENSP00000417918.1:n.*54T=
ENST00000471379.1:n.298T=
ENST00000497642.5:c.*54T=	ENSP00000418456.1:n.*54T=
NM_000340.1:c.587T=	NP_000331.1:p.Ile196=
NM_001278658.1:c.230T=	NP_001265587.1:p.Ile77=
NM_001278659.1:c.68T=	NP_001265588.1:p.Ile23=
XM_011513087.1:c.542T=	XP_011511389.1:p.Ile181=
XM_011513088.1:c.368T=	XP_011511390.1:p.Ile123=
XM_011513089.1:c.68T=	XP_011511391.1:p.Ile23=
XM_011513087.2:c.542T=	XP_011511389.1:p.Ile181=
XM_024453720.1:c.68T=	XP_024309488.1:p.Ile23=
NM_000340.2:c.587T= MANE Select	NP_000331.1:p.Ile196=
NM_001278658.2:c.230T=	NP_001265587.1:p.Ile77=
NM_001278659.2:c.68T=	NP_001265588.1:p.Ile23=