Canonical Allele Identifier: CA1538213148

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33954407G= , CM000667.2:g.33954407G=	GRCh38
NC_000005.9:g.33954512G= , CM000667.1:g.33954512G=	GRCh37
NC_000005.8:g.33990269G=	NCBI36
NG_011691.2:g.35269C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016180.5:c.986C= MANE Select	NP_057264.4:p.Thr329=
ENST00000296589.9:c.986C= MANE Select	ENSP00000296589.4:p.Thr329=
NM_001012509.3:c.986C=	NP_001012527.1:p.Thr329=
NM_001012509.4:c.986C=	NP_001012527.2:p.Thr329=
NM_001297417.2:c.660C=	NP_001284346.2:p.Asp220=
NM_001297417.3:c.660C=	NP_001284346.2:p.Asp220=
NM_001297417.4:c.660C=	NP_001284346.2:p.Asp220=
NM_016180.4:c.986C=	NP_057264.3:p.Thr329=
ENST00000296589.8:c.986C=	ENSP00000296589.4:p.Thr329=
ENST00000382102.7:c.986C=	ENSP00000371534.3:p.Thr329=
ENST00000509381.1:c.660C=	ENSP00000421100.1:p.Asp220=
ENST00000510600.1:c.461C=	ENSP00000424010.1:p.Thr154=
XM_011514051.1:c.584C=	XP_011512353.1:p.Thr195=
XR_925620.1:n.1803C=