Canonical Allele Identifier: CA2739277023
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2872877
ClinVar RCV Id: RCV003597704

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.761203delinsCTGAGGCAGCCGCTGAAAAGCACCCACGAGGCCACCTGCGGGGCCGGGAGGGAAGCGTAGG , CM000682.2:g.761203delinsCTGAGGCAGCCGCTGAAAAGCACCCACGAGGCCACCTGCGGGGCCGGGAGGGAAGCGTAGG GRCh38
NC_000020.10:g.741847delinsCTGAGGCAGCCGCTGAAAAGCACCCACGAGGCCACCTGCGGGGCCGGGAGGGAAGCGTAGG , CM000682.1:g.741847delinsCTGAGGCAGCCGCTGAAAAGCACCCACGAGGCCACCTGCGGGGCCGGGAGGGAAGCGTAGG GRCh37
NC_000020.9:g.689847delinsCTGAGGCAGCCGCTGAAAAGCACCCACGAGGCCACCTGCGGGGCCGGGAGGGAAGCGTAGG NCBI36
NG_027687.1:g.12382delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG
NG_027687.2:g.19783delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000381944.5:c.*447delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG ENSP00000371370.3:n.*447delinsCCTACGCTTCC...
ENST00000473664.2:c.727delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG ENSP00000502741.1:p.Leu243delinsProThrLeu...
ENST00000488495.3:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG ENSP00000494009.1:p.Ser411_Tyr412insLeuAr...
ENST00000645534.1:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG MANE Select ENSP00000494193.1:p.Ser411_Tyr412insLeuAr...
ENST00000217254.11:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG ENSP00000217254.7:p.Ser411_Tyr412insLeuAr...
ENST00000381944.4:c.*447delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG ENSP00000371370.3:n.*447delinsCCTACGCTTCC...
ENST00000473664.1:n.778delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG
ENST00000632431.1:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG ENSP00000488723.1:p.Ser411_Tyr412insLeuAr...
NM_033409.3:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG NP_212134.3:p.Ser411_Tyr412insLeuArgPhePr...
XM_005260655.3:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG XP_005260712.1:p.Ser411_Tyr412insLeuArgPh...
XM_011529148.1:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG XP_011527450.1:p.Ser411_Tyr412insLeuArgPh...
XM_005260655.4:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG XP_005260712.1:p.Ser411_Tyr412insLeuArgPh...
XM_024451821.1:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG XP_024307589.1:p.Ser411_Tyr412insLeuArgPh...
NM_033409.4:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG MANE Select NP_212134.3:p.Ser411_Tyr412insLeuArgPhePr...
NM_001370085.1:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG NP_001357014.1:p.Ser411_Tyr412insLeuArgPh...
NM_001370086.1:c.1233delinsCCTACGCTTCCCTCCCGGCCCCGCAGGTGGCCTCGTGGGTGCTTTTCAGCGGCTGCCTCAG NP_001357015.1:p.Ser411_Tyr412insLeuArgPh...