Canonical Allele Identifier: CA1538196199

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963937T= , CM000667.2:g.33963937T=	GRCh38
NC_000005.9:g.33964042T= , CM000667.1:g.33964042T=	GRCh37
NC_000005.8:g.33999799T=	NCBI36
NG_011691.2:g.25739A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.642A= MANE Select	ENSP00000296589.4:p.Glu214=
ENST00000296589.8:c.642A=	ENSP00000296589.4:p.Glu214=
ENST00000382102.7:c.642A=	ENSP00000371534.3:p.Glu214=
ENST00000505056.1:n.444A=
ENST00000509381.1:c.563-9433A=	ENSP00000421100.1:n.563-9433A=
ENST00000510600.1:c.117A=	ENSP00000424010.1:p.Glu39=
NM_001012509.3:c.642A=	NP_001012527.1:p.Glu214=
NM_001297417.2:c.563-9433A=	NP_001284346.2:n.563-9433A=
NM_016180.4:c.642A=	NP_057264.3:p.Glu214=
XM_011514051.1:c.240A=	XP_011512353.1:p.Glu80=
XM_011514052.1:c.642A=	XP_011512354.1:p.Glu214=
XR_925620.1:n.1459A=
NM_016180.5:c.642A= MANE Select	NP_057264.4:p.Glu214=
NM_001012509.4:c.642A=	NP_001012527.2:p.Glu214=
NM_001297417.3:c.563-9433A=	NP_001284346.2:n.563-9433A=
NM_001297417.4:c.563-9433A=	NP_001284346.2:n.563-9433A=