Canonical Allele Identifier: CA2651546190

Gene: SLC52A3

Linked Data

• gnomAD v4: 20-760750-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.760750C>A , CM000682.2:g.760750C>A	GRCh38
NC_000020.10:g.741394C>A , CM000682.1:g.741394C>A	GRCh37
NC_000020.9:g.689394C>A	NCBI36
NG_027687.1:g.12835G>T
NG_027687.2:g.20236G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381944.5:c.*900G>T	ENSP00000371370.3:n.*900G>T
ENST00000473664.2:c.*169G>T	ENSP00000502741.1:n.*169G>T
ENST00000488495.3:c.*276G>T	ENSP00000494009.1:n.*276G>T
ENST00000645534.1:c.*276G>T MANE Select	ENSP00000494193.1:n.*276G>T
ENST00000217254.11:c.*276G>T	ENSP00000217254.7:n.*276G>T
ENST00000381944.4:c.*900G>T	ENSP00000371370.3:n.*900G>T
ENST00000632431.1:c.*276G>T	ENSP00000488723.1:n.*276G>T
NM_033409.3:c.*276G>T	NP_212134.3:n.*276G>T
XM_005260655.3:c.*276G>T	XP_005260712.1:n.*276G>T
XM_011529148.1:c.*276G>T	XP_011527450.1:n.*276G>T
XM_005260655.4:c.*276G>T	XP_005260712.1:n.*276G>T
XM_024451821.1:c.*276G>T	XP_024307589.1:n.*276G>T
NM_033409.4:c.*276G>T MANE Select	NP_212134.3:n.*276G>T
NM_001370085.1:c.*276G>T	NP_001357014.1:n.*276G>T
NM_001370086.1:c.*276G>T	NP_001357015.1:n.*276G>T