Canonical Allele Identifier: CA339798

Gene: SLC52A3

Linked Data

• ClinVar Variation Id: 145
• ClinVar RCV Id: RCV000000168
• dbSNP Id: rs267606688
• MyVariant Identifiers: chr20:g.746337G>T (hg19) ; chr20:g.765693G>T (hg38)
• PubMed: PMID:20920669 ; PMID:26072523

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.765693G>T , CM000682.2:g.765693G>T	GRCh38
NC_000020.10:g.746337G>T , CM000682.1:g.746337G>T	GRCh37
NC_000020.9:g.694337G>T	NCBI36
NG_027687.1:g.7892C>A
NG_027687.2:g.15293C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381944.5:c.82C>A	ENSP00000371370.3:p.Pro28Thr
ENST00000473664.2:c.82C>A	ENSP00000502741.1:p.Pro28Thr
ENST00000488495.3:c.82C>A	ENSP00000494009.1:p.Pro28Thr
ENST00000645534.1:c.82C>A MANE Select	ENSP00000494193.1:p.Pro28Thr
ENST00000674666.1:c.82C>A	ENSP00000502783.1:p.Pro28Thr
ENST00000675066.1:c.82C>A	ENSP00000501902.1:p.Pro28Thr
ENST00000676154.1:c.82C>A	ENSP00000501807.1:p.Pro28Thr
ENST00000217254.11:c.82C>A	ENSP00000217254.7:p.Pro28Thr
ENST00000381944.4:c.82C>A	ENSP00000371370.3:p.Pro28Thr
ENST00000473664.1:n.133C>A
ENST00000632431.1:c.82C>A	ENSP00000488723.1:p.Pro28Thr
NM_033409.3:c.82C>A	NP_212134.3:p.Pro28Thr
XM_005260655.3:c.82C>A	XP_005260712.1:p.Pro28Thr
XM_011529148.1:c.82C>A	XP_011527450.1:p.Pro28Thr
XM_005260655.4:c.82C>A	XP_005260712.1:p.Pro28Thr
XM_024451821.1:c.82C>A	XP_024307589.1:p.Pro28Thr
NM_033409.4:c.82C>A MANE Select	NP_212134.3:p.Pro28Thr
NM_001370085.1:c.82C>A	NP_001357014.1:p.Pro28Thr
NM_001370086.1:c.82C>A	NP_001357015.1:p.Pro28Thr