Canonical Allele Identifier: CA2578282378

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964044dup , CM000667.2:g.33964044dup	GRCh38
NC_000005.9:g.33964149dup , CM000667.1:g.33964149dup	GRCh37
NC_000005.8:g.33999906dup	NCBI36
NG_011691.2:g.25632dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-28dup MANE Select	ENSP00000296589.4:n.563-28dup
ENST00000296589.8:c.563-28dup	ENSP00000296589.4:n.563-28dup
ENST00000382102.7:c.563-28dup	ENSP00000371534.3:n.563-28dup
ENST00000505056.1:n.365-28dup
ENST00000509381.1:c.563-9540dup	ENSP00000421100.1:n.563-9540dup
ENST00000510600.1:c.38-28dup	ENSP00000424010.1:n.38-28dup
NM_001012509.3:c.563-28dup	NP_001012527.1:n.563-28dup
NM_001297417.2:c.563-9540dup	NP_001284346.2:n.563-9540dup
NM_016180.4:c.563-28dup	NP_057264.3:n.563-28dup
XM_011514051.1:c.161-28dup	XP_011512353.1:n.161-28dup
XM_011514052.1:c.563-28dup	XP_011512354.1:n.563-28dup
XR_925620.1:n.1380-28dup
NM_016180.5:c.563-28dup MANE Select	NP_057264.4:n.563-28dup
NM_001012509.4:c.563-28dup	NP_001012527.2:n.563-28dup
NM_001297417.3:c.563-9540dup	NP_001284346.2:n.563-9540dup
NM_001297417.4:c.563-9540dup	NP_001284346.2:n.563-9540dup