Canonical Allele Identifier: CA407963729
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1391904
ClinVar RCV Id: RCV001893326
dbSNP Id: rs2122524593

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.765284G>T , CM000682.2:g.765284G>T GRCh38
NC_000020.10:g.745928G>T , CM000682.1:g.745928G>T GRCh37
NC_000020.9:g.693928G>T NCBI36
NG_027687.1:g.8301C>A
NG_027687.2:g.15702C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381944.5:c.491C>A ENSP00000371370.3:p.Thr164Asn
ENST00000473664.2:c.491C>A ENSP00000502741.1:p.Thr164Asn
ENST00000488495.3:c.491C>A ENSP00000494009.1:p.Thr164Asn
ENST00000645534.1:c.491C>A MANE Select ENSP00000494193.1:p.Thr164Asn
ENST00000675066.1:c.491C>A ENSP00000501902.1:p.Thr164Asn
ENST00000676154.1:c.491C>A ENSP00000501807.1:p.Thr164Asn
ENST00000217254.11:c.491C>A ENSP00000217254.7:p.Thr164Asn
ENST00000381944.4:c.491C>A ENSP00000371370.3:p.Thr164Asn
ENST00000473664.1:n.542C>A
ENST00000632431.1:c.491C>A ENSP00000488723.1:p.Thr164Asn
NM_033409.3:c.491C>A NP_212134.3:p.Thr164Asn
XM_005260655.3:c.491C>A XP_005260712.1:p.Thr164Asn
XM_011529148.1:c.491C>A XP_011527450.1:p.Thr164Asn
XM_005260655.4:c.491C>A XP_005260712.1:p.Thr164Asn
XM_024451821.1:c.491C>A XP_024307589.1:p.Thr164Asn
NM_033409.4:c.491C>A MANE Select NP_212134.3:p.Thr164Asn
NM_001370085.1:c.491C>A NP_001357014.1:p.Thr164Asn
NM_001370086.1:c.491C>A NP_001357015.1:p.Thr164Asn