Canonical Allele Identifier: CA1538196235

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963952T= , CM000667.2:g.33963952T=	GRCh38
NC_000005.9:g.33964057T= , CM000667.1:g.33964057T=	GRCh37
NC_000005.8:g.33999814T=	NCBI36
NG_011691.2:g.25724A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.627A= MANE Select	ENSP00000296589.4:p.Arg209=
ENST00000296589.8:c.627A=	ENSP00000296589.4:p.Arg209=
ENST00000382102.7:c.627A=	ENSP00000371534.3:p.Arg209=
ENST00000505056.1:n.429A=
ENST00000509381.1:c.563-9448A=	ENSP00000421100.1:n.563-9448A=
ENST00000510600.1:c.102A=	ENSP00000424010.1:p.Arg34=
NM_001012509.3:c.627A=	NP_001012527.1:p.Arg209=
NM_001297417.2:c.563-9448A=	NP_001284346.2:n.563-9448A=
NM_016180.4:c.627A=	NP_057264.3:p.Arg209=
XM_011514051.1:c.225A=	XP_011512353.1:p.Arg75=
XM_011514052.1:c.627A=	XP_011512354.1:p.Arg209=
XR_925620.1:n.1444A=
NM_016180.5:c.627A= MANE Select	NP_057264.4:p.Arg209=
NM_001012509.4:c.627A=	NP_001012527.2:p.Arg209=
NM_001297417.3:c.563-9448A=	NP_001284346.2:n.563-9448A=
NM_001297417.4:c.563-9448A=	NP_001284346.2:n.563-9448A=