Canonical Allele Identifier: CA407962689

Gene: SLC52A3

Linked Data

• ClinVar Variation Id: 1315574
• ClinVar RCV Id: RCV001774819
• dbSNP Id: rs2122516296
• COSMIC: COSM4727589 ; COSM4727590
• MyVariant Identifiers: chr20:g.744229T>C (hg19) ; chr20:g.763585T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.763585T>C , CM000682.2:g.763585T>C	GRCh38
NC_000020.10:g.744229T>C , CM000682.1:g.744229T>C	GRCh37
NC_000020.9:g.692229T>C	NCBI36
NG_027687.1:g.10000A>G
NG_027687.2:g.17401A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381944.5:c.986A>G	ENSP00000371370.3:p.Tyr329Cys
ENST00000473664.2:c.567+1623A>G	ENSP00000502741.1:n.567+1623A>G
ENST00000488495.3:c.986A>G	ENSP00000494009.1:p.Tyr329Cys
ENST00000645534.1:c.986A>G MANE Select	ENSP00000494193.1:p.Tyr329Cys
ENST00000675066.1:c.986A>G	ENSP00000501902.1:p.Tyr329Cys
ENST00000217254.11:c.986A>G	ENSP00000217254.7:p.Tyr329Cys
ENST00000381944.4:c.986A>G	ENSP00000371370.3:p.Tyr329Cys
ENST00000473664.1:n.618+1623A>G
ENST00000632431.1:c.986A>G	ENSP00000488723.1:p.Tyr329Cys
NM_033409.3:c.986A>G	NP_212134.3:p.Tyr329Cys
XM_005260655.3:c.986A>G	XP_005260712.1:p.Tyr329Cys
XM_011529148.1:c.986A>G	XP_011527450.1:p.Tyr329Cys
XM_005260655.4:c.986A>G	XP_005260712.1:p.Tyr329Cys
XM_024451821.1:c.986A>G	XP_024307589.1:p.Tyr329Cys
NM_033409.4:c.986A>G MANE Select	NP_212134.3:p.Tyr329Cys
NM_001370085.1:c.986A>G	NP_001357014.1:p.Tyr329Cys
NM_001370086.1:c.986A>G	NP_001357015.1:p.Tyr329Cys