Canonical Allele Identifier: CA1538189790

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33958897_33958898delinsAG , CM000667.2:g.33958897_33958898delinsAG	GRCh38
NC_000005.9:g.33959002_33959003delinsAG , CM000667.1:g.33959002_33959003delinsAG	GRCh37
NC_000005.8:g.33994759_33994760delinsAG	NCBI36
NG_011691.2:g.30778_30779delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-4394_889-4393delinsCT MANE Select	ENSP00000296589.4:n.889-4394_889-4393delinsCT
ENST00000296589.8:c.889-4394_889-4393delinsCT	ENSP00000296589.4:n.889-4394_889-4393delinsCT
ENST00000382102.7:c.889-4394_889-4393delinsCT	ENSP00000371534.3:n.889-4394_889-4393delinsCT
ENST00000509381.1:c.563-4394_563-4393delinsCT	ENSP00000421100.1:n.563-4394_563-4393delinsCT
ENST00000510600.1:c.364-4394_364-4393delinsCT	ENSP00000424010.1:n.364-4394_364-4393delinsCT
NM_001012509.3:c.889-4394_889-4393delinsCT	NP_001012527.1:n.889-4394_889-4393delinsCT
NM_001297417.2:c.563-4394_563-4393delinsCT	NP_001284346.2:n.563-4394_563-4393delinsCT
NM_016180.4:c.889-4394_889-4393delinsCT	NP_057264.3:n.889-4394_889-4393delinsCT
XM_011514051.1:c.487-4394_487-4393delinsCT	XP_011512353.1:n.487-4394_487-4393delinsCT
XR_925620.1:n.1706-4394_1706-4393delinsCT
NM_016180.5:c.889-4394_889-4393delinsCT MANE Select	NP_057264.4:n.889-4394_889-4393delinsCT
NM_001012509.4:c.889-4394_889-4393delinsCT	NP_001012527.2:n.889-4394_889-4393delinsCT
NM_001297417.3:c.563-4394_563-4393delinsCT	NP_001284346.2:n.563-4394_563-4393delinsCT
NM_001297417.4:c.563-4394_563-4393delinsCT	NP_001284346.2:n.563-4394_563-4393delinsCT