Canonical Allele Identifier: CA355485905

Gene: SLC2A2

Linked Data

• COSMIC: COSM141065
• MyVariant Identifiers: chr3:g.170716101G>A (hg19) ; chr3:g.170998312G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170998312G>A , CM000665.2:g.170998312G>A	GRCh38
NC_000003.11:g.170716101G>A , CM000665.1:g.170716101G>A	GRCh37
NC_000003.10:g.172198795G>A	NCBI36
NG_008108.1:g.33668C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.1255C>T MANE Select	ENSP00000323568.3:p.Pro419Ser
ENST00000314251.7:c.1255C>T	ENSP00000323568.3:p.Pro419Ser
ENST00000469787.1:c.*722C>T	ENSP00000417918.1:n.*722C>T
ENST00000497642.5:c.*722C>T	ENSP00000418456.1:n.*722C>T
NM_000340.1:c.1255C>T	NP_000331.1:p.Pro419Ser
NM_001278658.1:c.898C>T	NP_001265587.1:p.Pro300Ser
NM_001278659.1:c.736C>T	NP_001265588.1:p.Pro246Ser
XM_011513087.1:c.1210C>T	XP_011511389.1:p.Pro404Ser
XM_011513088.1:c.1036C>T	XP_011511390.1:p.Pro346Ser
XM_011513089.1:c.736C>T	XP_011511391.1:p.Pro246Ser
XM_011513087.2:c.1210C>T	XP_011511389.1:p.Pro404Ser
XM_024453720.1:c.736C>T	XP_024309488.1:p.Pro246Ser
NM_000340.2:c.1255C>T MANE Select	NP_000331.1:p.Pro419Ser
NM_001278658.2:c.898C>T	NP_001265587.1:p.Pro300Ser
NM_001278659.2:c.736C>T	NP_001265588.1:p.Pro246Ser