Canonical Allele Identifier: CA87706139

Gene: SLC2A2

Linked Data

• dbSNP Id: rs761552714
• gnomAD v3: 3-170999638-C-T
• gnomAD v4: 3-170999638-C-T
• MyVariant Identifiers: chr3:g.170717427C>T (hg19) ; chr3:g.170999638C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170999638C>T , CM000665.2:g.170999638C>T	GRCh38
NC_000003.11:g.170717427C>T , CM000665.1:g.170717427C>T	GRCh37
NC_000003.10:g.172200121C>T	NCBI36
NG_008108.1:g.32342G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.1069-472G>A MANE Select	ENSP00000323568.3:n.1069-472G>A
ENST00000314251.7:c.1069-472G>A	ENSP00000323568.3:n.1069-472G>A
ENST00000469787.1:c.*536-472G>A	ENSP00000417918.1:n.*536-472G>A
ENST00000497642.5:c.*536-472G>A	ENSP00000418456.1:n.*536-472G>A
NM_000340.1:c.1069-472G>A	NP_000331.1:n.1069-472G>A
NM_001278658.1:c.712-472G>A	NP_001265587.1:n.712-472G>A
NM_001278659.1:c.550-472G>A	NP_001265588.1:n.550-472G>A
XM_011513087.1:c.1024-472G>A	XP_011511389.1:n.1024-472G>A
XM_011513088.1:c.850-472G>A	XP_011511390.1:n.850-472G>A
XM_011513089.1:c.550-472G>A	XP_011511391.1:n.550-472G>A
XM_011513087.2:c.1024-472G>A	XP_011511389.1:n.1024-472G>A
XM_024453720.1:c.550-472G>A	XP_024309488.1:n.550-472G>A
NM_000340.2:c.1069-472G>A MANE Select	NP_000331.1:n.1069-472G>A
NM_001278658.2:c.712-472G>A	NP_001265587.1:n.712-472G>A
NM_001278659.2:c.550-472G>A	NP_001265588.1:n.550-472G>A