Canonical Allele Identifier: CA2765834626

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964052_33964053del , CM000667.2:g.33964052_33964053del	GRCh38
NC_000005.9:g.33964157_33964158del , CM000667.1:g.33964157_33964158del	GRCh37
NC_000005.8:g.33999914_33999915del	NCBI36
NG_011691.2:g.25623_25624del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-37_563-36del MANE Select	ENSP00000296589.4:n.563-37_563-36del
ENST00000296589.8:c.563-37_563-36del	ENSP00000296589.4:n.563-37_563-36del
ENST00000382102.7:c.563-37_563-36del	ENSP00000371534.3:n.563-37_563-36del
ENST00000505056.1:n.365-37_365-36del
ENST00000509381.1:c.563-9549_563-9548del	ENSP00000421100.1:n.563-9549_563-9548del
ENST00000510600.1:c.38-37_38-36del	ENSP00000424010.1:n.38-37_38-36del
NM_001012509.3:c.563-37_563-36del	NP_001012527.1:n.563-37_563-36del
NM_001297417.2:c.563-9549_563-9548del	NP_001284346.2:n.563-9549_563-9548del
NM_016180.4:c.563-37_563-36del	NP_057264.3:n.563-37_563-36del
XM_011514051.1:c.161-37_161-36del	XP_011512353.1:n.161-37_161-36del
XM_011514052.1:c.563-37_563-36del	XP_011512354.1:n.563-37_563-36del
XR_925620.1:n.1380-37_1380-36del
NM_016180.5:c.563-37_563-36del MANE Select	NP_057264.4:n.563-37_563-36del
NM_001012509.4:c.563-37_563-36del	NP_001012527.2:n.563-37_563-36del
NM_001297417.3:c.563-9549_563-9548del	NP_001284346.2:n.563-9549_563-9548del
NM_001297417.4:c.563-9549_563-9548del	NP_001284346.2:n.563-9549_563-9548del