Canonical Allele Identifier: CA2651547696

Gene: SLC52A3

Linked Data

• gnomAD v4: 20-764020-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.764020A>C , CM000682.2:g.764020A>C	GRCh38
NC_000020.10:g.744664A>C , CM000682.1:g.744664A>C	GRCh37
NC_000020.9:g.692664A>C	NCBI36
NG_027687.1:g.9565T>G
NG_027687.2:g.16966T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381944.5:c.568-17T>G	ENSP00000371370.3:n.568-17T>G
ENST00000473664.2:c.567+1188T>G	ENSP00000502741.1:n.567+1188T>G
ENST00000488495.3:c.568-17T>G	ENSP00000494009.1:n.568-17T>G
ENST00000645534.1:c.568-17T>G MANE Select	ENSP00000494193.1:n.568-17T>G
ENST00000675066.1:c.568-17T>G	ENSP00000501902.1:n.568-17T>G
ENST00000676154.1:c.568-17T>G	ENSP00000501807.1:n.568-17T>G
ENST00000217254.11:c.568-17T>G	ENSP00000217254.7:n.568-17T>G
ENST00000381944.4:c.568-17T>G	ENSP00000371370.3:n.568-17T>G
ENST00000473664.1:n.618+1188T>G
ENST00000632431.1:c.568-17T>G	ENSP00000488723.1:n.568-17T>G
NM_033409.3:c.568-17T>G	NP_212134.3:n.568-17T>G
XM_005260655.3:c.568-17T>G	XP_005260712.1:n.568-17T>G
XM_011529148.1:c.568-17T>G	XP_011527450.1:n.568-17T>G
XM_005260655.4:c.568-17T>G	XP_005260712.1:n.568-17T>G
XM_024451821.1:c.568-17T>G	XP_024307589.1:n.568-17T>G
NM_033409.4:c.568-17T>G MANE Select	NP_212134.3:n.568-17T>G
NM_001370085.1:c.568-17T>G	NP_001357014.1:n.568-17T>G
NM_001370086.1:c.568-17T>G	NP_001357015.1:n.568-17T>G