Canonical Allele Identifier: CA9724664

Gene: SLC52A3

Linked Data

• ClinVar Variation Id: 934011
• ClinVar RCV Id: RCV001202337 ; RCV001586041 ; RCV002375128
• dbSNP Id: rs142265627
• ExAC: 20:744350 C / T
• gnomAD v2: 20-744350-C-T
• gnomAD v3: 20-763706-C-T
• gnomAD v4: 20-763706-C-T
• MyVariant Identifiers: chr20:g.744350C>T (hg19) ; chr20:g.763706C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.763706C>T , CM000682.2:g.763706C>T	GRCh38
NC_000020.10:g.744350C>T , CM000682.1:g.744350C>T	GRCh37
NC_000020.9:g.692350C>T	NCBI36
NG_027687.1:g.9879G>A
NG_027687.2:g.17280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381944.5:c.865G>A	ENSP00000371370.3:p.Glu289Lys
ENST00000473664.2:c.567+1502G>A	ENSP00000502741.1:n.567+1502G>A
ENST00000488495.3:c.865G>A	ENSP00000494009.1:p.Glu289Lys
ENST00000645534.1:c.865G>A MANE Select	ENSP00000494193.1:p.Glu289Lys
ENST00000675066.1:c.865G>A	ENSP00000501902.1:p.Glu289Lys
ENST00000217254.11:c.865G>A	ENSP00000217254.7:p.Glu289Lys
ENST00000381944.4:c.865G>A	ENSP00000371370.3:p.Glu289Lys
ENST00000473664.1:n.618+1502G>A
ENST00000632431.1:c.865G>A	ENSP00000488723.1:p.Glu289Lys
NM_033409.3:c.865G>A	NP_212134.3:p.Glu289Lys
XM_005260655.3:c.865G>A	XP_005260712.1:p.Glu289Lys
XM_011529148.1:c.865G>A	XP_011527450.1:p.Glu289Lys
XM_005260655.4:c.865G>A	XP_005260712.1:p.Glu289Lys
XM_024451821.1:c.865G>A	XP_024307589.1:p.Glu289Lys
NM_033409.4:c.865G>A MANE Select	NP_212134.3:p.Glu289Lys
NM_001370085.1:c.865G>A	NP_001357014.1:p.Glu289Lys
NM_001370086.1:c.865G>A	NP_001357015.1:p.Glu289Lys