Canonical Allele Identifier: CA1538213602

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33955426G= , CM000667.2:g.33955426G=	GRCh38
NC_000005.9:g.33955531G= , CM000667.1:g.33955531G=	GRCh37
NC_000005.8:g.33991288G=	NCBI36
NG_011691.2:g.34250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-922C= MANE Select	ENSP00000296589.4:n.889-922C=
ENST00000296589.8:c.889-922C=	ENSP00000296589.4:n.889-922C=
ENST00000382102.7:c.889-922C=	ENSP00000371534.3:n.889-922C=
ENST00000509381.1:c.563-922C=	ENSP00000421100.1:n.563-922C=
ENST00000510600.1:c.364-922C=	ENSP00000424010.1:n.364-922C=
NM_001012509.3:c.889-922C=	NP_001012527.1:n.889-922C=
NM_001297417.2:c.563-922C=	NP_001284346.2:n.563-922C=
NM_016180.4:c.889-922C=	NP_057264.3:n.889-922C=
XM_011514051.1:c.487-922C=	XP_011512353.1:n.487-922C=
XR_925620.1:n.1706-922C=
NM_016180.5:c.889-922C= MANE Select	NP_057264.4:n.889-922C=
NM_001012509.4:c.889-922C=	NP_001012527.2:n.889-922C=
NM_001297417.3:c.563-922C=	NP_001284346.2:n.563-922C=
NM_001297417.4:c.563-922C=	NP_001284346.2:n.563-922C=