Canonical Allele Identifier: CA1538211633

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951475T= , CM000667.2:g.33951475T=	GRCh38
NC_000005.9:g.33951580T= , CM000667.1:g.33951580T=	GRCh37
NC_000005.8:g.33987337T=	NCBI36
NG_011691.2:g.38201A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1156+79A= MANE Select	ENSP00000296589.4:n.1156+79A=
ENST00000296589.8:c.1156+79A=	ENSP00000296589.4:n.1156+79A=
ENST00000382102.7:c.1156+79A=	ENSP00000371534.3:n.1156+79A=
ENST00000509381.1:c.*177A=	ENSP00000421100.1:n.*177A=
ENST00000510600.1:c.631+79A=	ENSP00000424010.1:n.631+79A=
NM_001012509.3:c.1156+79A=	NP_001012527.1:n.1156+79A=
NM_001297417.2:c.*177A=	NP_001284346.2:n.*177A=
NM_016180.4:c.1156+79A=	NP_057264.3:n.1156+79A=
XM_011514051.1:c.754+79A=	XP_011512353.1:n.754+79A=
XR_925620.1:n.1973+79A=
NM_016180.5:c.1156+79A= MANE Select	NP_057264.4:n.1156+79A=
NM_001012509.4:c.1156+79A=	NP_001012527.2:n.1156+79A=
NM_001297417.3:c.*177A=	NP_001284346.2:n.*177A=
NM_001297417.4:c.*177A=	NP_001284346.2:n.*177A=