Canonical Allele Identifier: CA1420161894

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170998316C= , CM000665.2:g.170998316C=	GRCh38
NC_000003.11:g.170716105C= , CM000665.1:g.170716105C=	GRCh37
NC_000003.10:g.172198799C=	NCBI36
NG_008108.1:g.33664G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.1251G= MANE Select	ENSP00000323568.3:p.Pro417=
ENST00000314251.7:c.1251G=	ENSP00000323568.3:p.Pro417=
ENST00000469787.1:c.*718G=	ENSP00000417918.1:n.*718G=
ENST00000497642.5:c.*718G=	ENSP00000418456.1:n.*718G=
NM_000340.1:c.1251G=	NP_000331.1:p.Pro417=
NM_001278658.1:c.894G=	NP_001265587.1:p.Pro298=
NM_001278659.1:c.732G=	NP_001265588.1:p.Pro244=
XM_011513087.1:c.1206G=	XP_011511389.1:p.Pro402=
XM_011513088.1:c.1032G=	XP_011511390.1:p.Pro344=
XM_011513089.1:c.732G=	XP_011511391.1:p.Pro244=
XM_011513087.2:c.1206G=	XP_011511389.1:p.Pro402=
XM_024453720.1:c.732G=	XP_024309488.1:p.Pro244=
NM_000340.2:c.1251G= MANE Select	NP_000331.1:p.Pro417=
NM_001278658.2:c.894G=	NP_001265587.1:p.Pro298=
NM_001278659.2:c.732G=	NP_001265588.1:p.Pro244=