Canonical Allele Identifier: CA1538189259

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1752342905

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33958510del , CM000667.2:g.33958510del	GRCh38
NC_000005.9:g.33958615del , CM000667.1:g.33958615del	GRCh37
NC_000005.8:g.33994372del	NCBI36
NG_011691.2:g.31166del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-4006del MANE Select	ENSP00000296589.4:n.889-4006del
ENST00000296589.8:c.889-4006del	ENSP00000296589.4:n.889-4006del
ENST00000382102.7:c.889-4006del	ENSP00000371534.3:n.889-4006del
ENST00000509381.1:c.563-4006del	ENSP00000421100.1:n.563-4006del
ENST00000510600.1:c.364-4006del	ENSP00000424010.1:n.364-4006del
NM_001012509.3:c.889-4006del	NP_001012527.1:n.889-4006del
NM_001297417.2:c.563-4006del	NP_001284346.2:n.563-4006del
NM_016180.4:c.889-4006del	NP_057264.3:n.889-4006del
XM_011514051.1:c.487-4006del	XP_011512353.1:n.487-4006del
XR_925620.1:n.1706-4006del
NM_016180.5:c.889-4006del MANE Select	NP_057264.4:n.889-4006del
NM_001012509.4:c.889-4006del	NP_001012527.2:n.889-4006del
NM_001297417.3:c.563-4006del	NP_001284346.2:n.563-4006del
NM_001297417.4:c.563-4006del	NP_001284346.2:n.563-4006del