Canonical Allele Identifier: CA1420168526

Gene: SLC2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171014511G= , CM000665.2:g.171014511G=	GRCh38
NC_000003.11:g.170732300G= , CM000665.1:g.170732300G=	GRCh37
NC_000003.10:g.172214994G=	NCBI36
NG_008108.1:g.17469C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000340.2:c.329C= MANE Select	NP_000331.1:p.Thr110=
ENST00000314251.8:c.329C= MANE Select	ENSP00000323568.3:p.Thr110=
NM_000340.1:c.329C=	NP_000331.1:p.Thr110=
NM_001278658.1:c.14+4020C=	NP_001265587.1:n.14+4020C=
NM_001278658.2:c.14+4020C=	NP_001265587.1:n.14+4020C=
NM_001278659.1:c.-66C=	NP_001265588.1:n.-66C=
NM_001278659.2:c.-66C=	NP_001265588.1:n.-66C=
ENST00000314251.7:c.329C=	ENSP00000323568.3:p.Thr110=
ENST00000461867.1:c.-24+4020C=	ENSP00000418888.1:n.-24+4020C=
ENST00000469787.1:c.108+4020C=	ENSP00000417918.1:n.108+4020C=
ENST00000497642.5:c.329C=	ENSP00000418456.1:p.Thr110=
XM_011513087.1:c.284C=	XP_011511389.1:p.Thr95=
XM_011513087.2:c.284C=	XP_011511389.1:p.Thr95=
XM_011513088.1:c.110C=	XP_011511390.1:p.Thr37=
XM_011513089.1:c.-24+4020C=	XP_011511391.1:n.-24+4020C=
XM_024453720.1:c.-24+4020C=	XP_024309488.1:n.-24+4020C=