Canonical Allele Identifier: CA1420165563

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007177C= , CM000665.2:g.171007177C=	GRCh38
NC_000003.11:g.170724966C= , CM000665.1:g.170724966C=	GRCh37
NC_000003.10:g.172207660C=	NCBI36
NG_008108.1:g.24803G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.583G= MANE Select	ENSP00000323568.3:p.Ala195=
ENST00000314251.7:c.583G=	ENSP00000323568.3:p.Ala195=
ENST00000461867.1:c.64G=	ENSP00000418888.1:p.Ala22=
ENST00000469787.1:c.*50G=	ENSP00000417918.1:n.*50G=
ENST00000471379.1:n.294G=
ENST00000497642.5:c.*50G=	ENSP00000418456.1:n.*50G=
NM_000340.1:c.583G=	NP_000331.1:p.Ala195=
NM_001278658.1:c.226G=	NP_001265587.1:p.Ala76=
NM_001278659.1:c.64G=	NP_001265588.1:p.Ala22=
XM_011513087.1:c.538G=	XP_011511389.1:p.Ala180=
XM_011513088.1:c.364G=	XP_011511390.1:p.Ala122=
XM_011513089.1:c.64G=	XP_011511391.1:p.Ala22=
XM_011513087.2:c.538G=	XP_011511389.1:p.Ala180=
XM_024453720.1:c.64G=	XP_024309488.1:p.Ala22=
NM_000340.2:c.583G= MANE Select	NP_000331.1:p.Ala195=
NM_001278658.2:c.226G=	NP_001265587.1:p.Ala76=
NM_001278659.2:c.64G=	NP_001265588.1:p.Ala22=