Canonical Allele Identifier: CA407962735
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002269
ClinVar RCV Id: RCV001298670
dbSNP Id: rs1986562969
gnomAD v4: 20-763606-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.763606T>C , CM000682.2:g.763606T>C GRCh38
NC_000020.10:g.744250T>C , CM000682.1:g.744250T>C GRCh37
NC_000020.9:g.692250T>C NCBI36
NG_027687.1:g.9979A>G
NG_027687.2:g.17380A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381944.5:c.965A>G ENSP00000371370.3:p.Gln322Arg
ENST00000473664.2:c.567+1602A>G ENSP00000502741.1:n.567+1602A>G
ENST00000488495.3:c.965A>G ENSP00000494009.1:p.Gln322Arg
ENST00000645534.1:c.965A>G MANE Select ENSP00000494193.1:p.Gln322Arg
ENST00000675066.1:c.965A>G ENSP00000501902.1:p.Gln322Arg
ENST00000217254.11:c.965A>G ENSP00000217254.7:p.Gln322Arg
ENST00000381944.4:c.965A>G ENSP00000371370.3:p.Gln322Arg
ENST00000473664.1:n.618+1602A>G
ENST00000632431.1:c.965A>G ENSP00000488723.1:p.Gln322Arg
NM_033409.3:c.965A>G NP_212134.3:p.Gln322Arg
XM_005260655.3:c.965A>G XP_005260712.1:p.Gln322Arg
XM_011529148.1:c.965A>G XP_011527450.1:p.Gln322Arg
XM_005260655.4:c.965A>G XP_005260712.1:p.Gln322Arg
XM_024451821.1:c.965A>G XP_024307589.1:p.Gln322Arg
NM_033409.4:c.965A>G MANE Select NP_212134.3:p.Gln322Arg
NM_001370085.1:c.965A>G NP_001357014.1:p.Gln322Arg
NM_001370086.1:c.965A>G NP_001357015.1:p.Gln322Arg