Canonical Allele Identifier: CA1538195969

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963786T= , CM000667.2:g.33963786T=	GRCh38
NC_000005.9:g.33963891T= , CM000667.1:g.33963891T=	GRCh37
NC_000005.8:g.33999648T=	NCBI36
NG_011691.2:g.25890A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.793A= MANE Select	ENSP00000296589.4:p.Met265=
ENST00000296589.8:c.793A=	ENSP00000296589.4:p.Met265=
ENST00000382102.7:c.793A=	ENSP00000371534.3:p.Met265=
ENST00000505056.1:n.595A=
ENST00000509381.1:c.563-9282A=	ENSP00000421100.1:n.563-9282A=
ENST00000510600.1:c.268A=	ENSP00000424010.1:p.Met90=
NM_001012509.3:c.793A=	NP_001012527.1:p.Met265=
NM_001297417.2:c.563-9282A=	NP_001284346.2:n.563-9282A=
NM_016180.4:c.793A=	NP_057264.3:p.Met265=
XM_011514051.1:c.391A=	XP_011512353.1:p.Met131=
XM_011514052.1:c.793A=	XP_011512354.1:p.Met265=
XR_925620.1:n.1610A=
NM_016180.5:c.793A= MANE Select	NP_057264.4:p.Met265=
NM_001012509.4:c.793A=	NP_001012527.2:p.Met265=
NM_001297417.3:c.563-9282A=	NP_001284346.2:n.563-9282A=
NM_001297417.4:c.563-9282A=	NP_001284346.2:n.563-9282A=