Canonical Allele Identifier: CA2345348095

Gene: SLC52A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.761110G= , CM000682.2:g.761110G=	GRCh38
NC_000020.10:g.741754G= , CM000682.1:g.741754G=	GRCh37
NC_000020.9:g.689754G=	NCBI36
NG_027687.1:g.12475C=
NG_027687.2:g.19876C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381944.5:c.*540C=	ENSP00000371370.3:n.*540C=
ENST00000473664.2:c.820C=	ENSP00000502741.1:p.Arg274=
ENST00000488495.3:c.1326C=	ENSP00000494009.1:p.Leu442=
ENST00000645534.1:c.1326C= MANE Select	ENSP00000494193.1:p.Leu442=
ENST00000217254.11:c.1326C=	ENSP00000217254.7:p.Leu442=
ENST00000381944.4:c.*540C=	ENSP00000371370.3:n.*540C=
ENST00000473664.1:n.871C=
ENST00000632431.1:c.1326C=	ENSP00000488723.1:p.Leu442=
NM_033409.3:c.1326C=	NP_212134.3:p.Leu442=
XM_005260655.3:c.1326C=	XP_005260712.1:p.Leu442=
XM_011529148.1:c.1326C=	XP_011527450.1:p.Leu442=
XM_005260655.4:c.1326C=	XP_005260712.1:p.Leu442=
XM_024451821.1:c.1326C=	XP_024307589.1:p.Leu442=
NM_033409.4:c.1326C= MANE Select	NP_212134.3:p.Leu442=
NM_001370085.1:c.1326C=	NP_001357014.1:p.Leu442=
NM_001370086.1:c.1326C=	NP_001357015.1:p.Leu442=