Canonical Allele Identifier: CA1420161859

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170998210A= , CM000665.2:g.170998210A=	GRCh38
NC_000003.11:g.170715999A= , CM000665.1:g.170715999A=	GRCh37
NC_000003.10:g.172198693A=	NCBI36
NG_008108.1:g.33770T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.1357T= MANE Select	ENSP00000323568.3:p.Cys453=
ENST00000314251.7:c.1357T=	ENSP00000323568.3:p.Cys453=
ENST00000469787.1:c.*824T=	ENSP00000417918.1:n.*824T=
ENST00000497642.5:c.*824T=	ENSP00000418456.1:n.*824T=
NM_000340.1:c.1357T=	NP_000331.1:p.Cys453=
NM_001278658.1:c.1000T=	NP_001265587.1:p.Cys334=
NM_001278659.1:c.838T=	NP_001265588.1:p.Cys280=
XM_011513087.1:c.1312T=	XP_011511389.1:p.Cys438=
XM_011513088.1:c.1138T=	XP_011511390.1:p.Cys380=
XM_011513089.1:c.838T=	XP_011511391.1:p.Cys280=
XM_011513087.2:c.1312T=	XP_011511389.1:p.Cys438=
XM_024453720.1:c.838T=	XP_024309488.1:p.Cys280=
NM_000340.2:c.1357T= MANE Select	NP_000331.1:p.Cys453=
NM_001278658.2:c.1000T=	NP_001265587.1:p.Cys334=
NM_001278659.2:c.838T=	NP_001265588.1:p.Cys280=