Canonical Allele Identifier: CA1538218469

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33984230A= , CM000667.2:g.33984230A=	GRCh38
NC_000005.9:g.33984335A= , CM000667.1:g.33984335A=	GRCh37
NC_000005.8:g.34020092A=	NCBI36
NG_011691.2:g.5446T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.354T= MANE Select	ENSP00000296589.4:p.Ala118=
ENST00000296589.8:c.354T=	ENSP00000296589.4:p.Ala118=
ENST00000382102.7:c.354T=	ENSP00000371534.3:p.Ala118=
ENST00000505056.1:n.333T=
ENST00000509381.1:c.354T=	ENSP00000421100.1:p.Ala118=
ENST00000510600.1:c.6T=	ENSP00000424010.1:p.Ala2=
NM_001012509.3:c.354T=	NP_001012527.1:p.Ala118=
NM_001297417.2:c.354T=	NP_001284346.2:p.Ala118=
NM_016180.4:c.354T=	NP_057264.3:p.Ala118=
XM_011514052.1:c.354T=	XP_011512354.1:p.Ala118=
XR_925620.1:n.915T=
NM_016180.5:c.354T= MANE Select	NP_057264.4:p.Ala118=
NM_001012509.4:c.354T=	NP_001012527.2:p.Ala118=
NM_001297417.3:c.354T=	NP_001284346.2:p.Ala118=
NM_001297417.4:c.354T=	NP_001284346.2:p.Ala118=