Canonical Allele Identifier: CA2345348013

Gene: SLC52A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.760985A= , CM000682.2:g.760985A=	GRCh38
NC_000020.10:g.741629A= , CM000682.1:g.741629A=	GRCh37
NC_000020.9:g.689629A=	NCBI36
NG_027687.1:g.12600T=
NG_027687.2:g.20001T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381944.5:c.*665T=	ENSP00000371370.3:n.*665T=
ENST00000473664.2:c.945T=	ENSP00000502741.1:p.Thr315=
ENST00000488495.3:c.*41T=	ENSP00000494009.1:n.*41T=
ENST00000645534.1:c.*41T= MANE Select	ENSP00000494193.1:n.*41T=
ENST00000217254.11:c.*41T=	ENSP00000217254.7:n.*41T=
ENST00000381944.4:c.*665T=	ENSP00000371370.3:n.*665T=
ENST00000632431.1:c.*41T=	ENSP00000488723.1:n.*41T=
NM_033409.3:c.*41T=	NP_212134.3:n.*41T=
XM_005260655.3:c.*41T=	XP_005260712.1:n.*41T=
XM_011529148.1:c.*41T=	XP_011527450.1:n.*41T=
XM_005260655.4:c.*41T=	XP_005260712.1:n.*41T=
XM_024451821.1:c.*41T=	XP_024307589.1:n.*41T=
NM_033409.4:c.*41T= MANE Select	NP_212134.3:n.*41T=
NM_001370085.1:c.*41T=	NP_001357014.1:n.*41T=
NM_001370086.1:c.*41T=	NP_001357015.1:n.*41T=