Canonical Allele Identifier: CA355485921

Gene: SLC2A2

Linked Data

• MyVariant Identifiers: chr3:g.170716109C>T (hg19) ; chr3:g.170998320C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170998320C>T , CM000665.2:g.170998320C>T	GRCh38
NC_000003.11:g.170716109C>T , CM000665.1:g.170716109C>T	GRCh37
NC_000003.10:g.172198803C>T	NCBI36
NG_008108.1:g.33660G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.1247G>A MANE Select	ENSP00000323568.3:p.Gly416Asp
ENST00000314251.7:c.1247G>A	ENSP00000323568.3:p.Gly416Asp
ENST00000469787.1:c.*714G>A	ENSP00000417918.1:n.*714G>A
ENST00000497642.5:c.*714G>A	ENSP00000418456.1:n.*714G>A
NM_000340.1:c.1247G>A	NP_000331.1:p.Gly416Asp
NM_001278658.1:c.890G>A	NP_001265587.1:p.Gly297Asp
NM_001278659.1:c.728G>A	NP_001265588.1:p.Gly243Asp
XM_011513087.1:c.1202G>A	XP_011511389.1:p.Gly401Asp
XM_011513088.1:c.1028G>A	XP_011511390.1:p.Gly343Asp
XM_011513089.1:c.728G>A	XP_011511391.1:p.Gly243Asp
XM_011513087.2:c.1202G>A	XP_011511389.1:p.Gly401Asp
XM_024453720.1:c.728G>A	XP_024309488.1:p.Gly243Asp
NM_000340.2:c.1247G>A MANE Select	NP_000331.1:p.Gly416Asp
NM_001278658.2:c.890G>A	NP_001265587.1:p.Gly297Asp
NM_001278659.2:c.728G>A	NP_001265588.1:p.Gly243Asp