Canonical Allele Identifier: CA1420162421

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170999684A= , CM000665.2:g.170999684A=	GRCh38
NC_000003.11:g.170717473A= , CM000665.1:g.170717473A=	GRCh37
NC_000003.10:g.172200167A=	NCBI36
NG_008108.1:g.32296T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.1069-518T= MANE Select	ENSP00000323568.3:n.1069-518T=
ENST00000314251.7:c.1069-518T=	ENSP00000323568.3:n.1069-518T=
ENST00000469787.1:c.*536-518T=	ENSP00000417918.1:n.*536-518T=
ENST00000497642.5:c.*536-518T=	ENSP00000418456.1:n.*536-518T=
NM_000340.1:c.1069-518T=	NP_000331.1:n.1069-518T=
NM_001278658.1:c.712-518T=	NP_001265587.1:n.712-518T=
NM_001278659.1:c.550-518T=	NP_001265588.1:n.550-518T=
XM_011513087.1:c.1024-518T=	XP_011511389.1:n.1024-518T=
XM_011513088.1:c.850-518T=	XP_011511390.1:n.850-518T=
XM_011513089.1:c.550-518T=	XP_011511391.1:n.550-518T=
XM_011513087.2:c.1024-518T=	XP_011511389.1:n.1024-518T=
XM_024453720.1:c.550-518T=	XP_024309488.1:n.550-518T=
NM_000340.2:c.1069-518T= MANE Select	NP_000331.1:n.1069-518T=
NM_001278658.2:c.712-518T=	NP_001265587.1:n.712-518T=
NM_001278659.2:c.550-518T=	NP_001265588.1:n.550-518T=