Canonical Allele Identifier: CA2765834710

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964077del , CM000667.2:g.33964077del	GRCh38
NC_000005.9:g.33964182del , CM000667.1:g.33964182del	GRCh37
NC_000005.8:g.33999939del	NCBI36
NG_011691.2:g.25599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-61del MANE Select	ENSP00000296589.4:n.563-61del
ENST00000296589.8:c.563-61del	ENSP00000296589.4:n.563-61del
ENST00000382102.7:c.563-61del	ENSP00000371534.3:n.563-61del
ENST00000505056.1:n.365-61del
ENST00000509381.1:c.563-9573del	ENSP00000421100.1:n.563-9573del
ENST00000510600.1:c.38-61del	ENSP00000424010.1:n.38-61del
NM_001012509.3:c.563-61del	NP_001012527.1:n.563-61del
NM_001297417.2:c.563-9573del	NP_001284346.2:n.563-9573del
NM_016180.4:c.563-61del	NP_057264.3:n.563-61del
XM_011514051.1:c.161-61del	XP_011512353.1:n.161-61del
XM_011514052.1:c.563-61del	XP_011512354.1:n.563-61del
XR_925620.1:n.1380-61del
NM_016180.5:c.563-61del MANE Select	NP_057264.4:n.563-61del
NM_001012509.4:c.563-61del	NP_001012527.2:n.563-61del
NM_001297417.3:c.563-9573del	NP_001284346.2:n.563-9573del
NM_001297417.4:c.563-9573del	NP_001284346.2:n.563-9573del