Canonical Allele Identifier: CA407961867

Gene: SLC52A3

Linked Data

• MyVariant Identifiers: chr20:g.741753C>A (hg19) ; chr20:g.761109C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.761109C>A , CM000682.2:g.761109C>A	GRCh38
NC_000020.10:g.741753C>A , CM000682.1:g.741753C>A	GRCh37
NC_000020.9:g.689753C>A	NCBI36
NG_027687.1:g.12476G>T
NG_027687.2:g.19877G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381944.5:c.*541G>T	ENSP00000371370.3:n.*541G>T
ENST00000473664.2:c.821G>T	ENSP00000502741.1:p.Arg274Leu
ENST00000488495.3:c.1327G>T	ENSP00000494009.1:p.Gly443Ter
ENST00000645534.1:c.1327G>T MANE Select	ENSP00000494193.1:p.Gly443Ter
ENST00000217254.11:c.1327G>T	ENSP00000217254.7:p.Gly443Ter
ENST00000381944.4:c.*541G>T	ENSP00000371370.3:n.*541G>T
ENST00000473664.1:n.872G>T
ENST00000632431.1:c.1327G>T	ENSP00000488723.1:p.Gly443Ter
NM_033409.3:c.1327G>T	NP_212134.3:p.Gly443Ter
XM_005260655.3:c.1327G>T	XP_005260712.1:p.Gly443Ter
XM_011529148.1:c.1327G>T	XP_011527450.1:p.Gly443Ter
XM_005260655.4:c.1327G>T	XP_005260712.1:p.Gly443Ter
XM_024451821.1:c.1327G>T	XP_024307589.1:p.Gly443Ter
NM_033409.4:c.1327G>T MANE Select	NP_212134.3:p.Gly443Ter
NM_001370085.1:c.1327G>T	NP_001357014.1:p.Gly443Ter
NM_001370086.1:c.1327G>T	NP_001357015.1:p.Gly443Ter