Canonical Allele Identifier: CA1420161856

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170998205G= , CM000665.2:g.170998205G=	GRCh38
NC_000003.11:g.170715994G= , CM000665.1:g.170715994G=	GRCh37
NC_000003.10:g.172198688G=	NCBI36
NG_008108.1:g.33775C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.1362C= MANE Select	ENSP00000323568.3:p.Phe454=
ENST00000314251.7:c.1362C=	ENSP00000323568.3:p.Phe454=
ENST00000469787.1:c.*829C=	ENSP00000417918.1:n.*829C=
ENST00000497642.5:c.*829C=	ENSP00000418456.1:n.*829C=
NM_000340.1:c.1362C=	NP_000331.1:p.Phe454=
NM_001278658.1:c.1005C=	NP_001265587.1:p.Phe335=
NM_001278659.1:c.843C=	NP_001265588.1:p.Phe281=
XM_011513087.1:c.1317C=	XP_011511389.1:p.Phe439=
XM_011513088.1:c.1143C=	XP_011511390.1:p.Phe381=
XM_011513089.1:c.843C=	XP_011511391.1:p.Phe281=
XM_011513087.2:c.1317C=	XP_011511389.1:p.Phe439=
XM_024453720.1:c.843C=	XP_024309488.1:p.Phe281=
NM_000340.2:c.1362C= MANE Select	NP_000331.1:p.Phe454=
NM_001278658.2:c.1005C=	NP_001265587.1:p.Phe335=
NM_001278659.2:c.843C=	NP_001265588.1:p.Phe281=