Canonical Allele Identifier: CA1538185346

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33955691T= , CM000667.2:g.33955691T=	GRCh38
NC_000005.9:g.33955796T= , CM000667.1:g.33955796T=	GRCh37
NC_000005.8:g.33991553T=	NCBI36
NG_011691.2:g.33985A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-1187A= MANE Select	ENSP00000296589.4:n.889-1187A=
ENST00000296589.8:c.889-1187A=	ENSP00000296589.4:n.889-1187A=
ENST00000382102.7:c.889-1187A=	ENSP00000371534.3:n.889-1187A=
ENST00000509381.1:c.563-1187A=	ENSP00000421100.1:n.563-1187A=
ENST00000510600.1:c.364-1187A=	ENSP00000424010.1:n.364-1187A=
NM_001012509.3:c.889-1187A=	NP_001012527.1:n.889-1187A=
NM_001297417.2:c.563-1187A=	NP_001284346.2:n.563-1187A=
NM_016180.4:c.889-1187A=	NP_057264.3:n.889-1187A=
XM_011514051.1:c.487-1187A=	XP_011512353.1:n.487-1187A=
XR_925620.1:n.1706-1187A=
NM_016180.5:c.889-1187A= MANE Select	NP_057264.4:n.889-1187A=
NM_001012509.4:c.889-1187A=	NP_001012527.2:n.889-1187A=
NM_001297417.3:c.563-1187A=	NP_001284346.2:n.563-1187A=
NM_001297417.4:c.563-1187A=	NP_001284346.2:n.563-1187A=