Canonical Allele Identifier: CA1538196278

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963968T= , CM000667.2:g.33963968T=	GRCh38
NC_000005.9:g.33964073T= , CM000667.1:g.33964073T=	GRCh37
NC_000005.8:g.33999830T=	NCBI36
NG_011691.2:g.25708A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.611A= MANE Select	ENSP00000296589.4:p.His204=
ENST00000296589.8:c.611A=	ENSP00000296589.4:p.His204=
ENST00000382102.7:c.611A=	ENSP00000371534.3:p.His204=
ENST00000505056.1:n.413A=
ENST00000509381.1:c.563-9464A=	ENSP00000421100.1:n.563-9464A=
ENST00000510600.1:c.86A=	ENSP00000424010.1:p.His29=
NM_001012509.3:c.611A=	NP_001012527.1:p.His204=
NM_001297417.2:c.563-9464A=	NP_001284346.2:n.563-9464A=
NM_016180.4:c.611A=	NP_057264.3:p.His204=
XM_011514051.1:c.209A=	XP_011512353.1:p.His70=
XM_011514052.1:c.611A=	XP_011512354.1:p.His204=
XR_925620.1:n.1428A=
NM_016180.5:c.611A= MANE Select	NP_057264.4:p.His204=
NM_001012509.4:c.611A=	NP_001012527.2:p.His204=
NM_001297417.3:c.563-9464A=	NP_001284346.2:n.563-9464A=
NM_001297417.4:c.563-9464A=	NP_001284346.2:n.563-9464A=