Canonical Allele Identifier: CA1538195940

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963780C= , CM000667.2:g.33963780C=	GRCh38
NC_000005.9:g.33963885C= , CM000667.1:g.33963885C=	GRCh37
NC_000005.8:g.33999642C=	NCBI36
NG_011691.2:g.25896G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.799G= MANE Select	ENSP00000296589.4:p.Glu267=
ENST00000296589.8:c.799G=	ENSP00000296589.4:p.Glu267=
ENST00000382102.7:c.799G=	ENSP00000371534.3:p.Glu267=
ENST00000505056.1:n.601G=
ENST00000509381.1:c.563-9276G=	ENSP00000421100.1:n.563-9276G=
ENST00000510600.1:c.274G=	ENSP00000424010.1:p.Glu92=
NM_001012509.3:c.799G=	NP_001012527.1:p.Glu267=
NM_001297417.2:c.563-9276G=	NP_001284346.2:n.563-9276G=
NM_016180.4:c.799G=	NP_057264.3:p.Glu267=
XM_011514051.1:c.397G=	XP_011512353.1:p.Glu133=
XM_011514052.1:c.799G=	XP_011512354.1:p.Glu267=
XR_925620.1:n.1616G=
NM_016180.5:c.799G= MANE Select	NP_057264.4:p.Glu267=
NM_001012509.4:c.799G=	NP_001012527.2:p.Glu267=
NM_001297417.3:c.563-9276G=	NP_001284346.2:n.563-9276G=
NM_001297417.4:c.563-9276G=	NP_001284346.2:n.563-9276G=