Canonical Allele Identifier: CA1538213582

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1752244325

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33955390_33955391del , CM000667.2:g.33955390_33955391del	GRCh38
NC_000005.9:g.33955495_33955496del , CM000667.1:g.33955495_33955496del	GRCh37
NC_000005.8:g.33991252_33991253del	NCBI36
NG_011691.2:g.34285_34286del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-887_889-886del MANE Select	ENSP00000296589.4:n.889-887_889-886del
ENST00000296589.8:c.889-887_889-886del	ENSP00000296589.4:n.889-887_889-886del
ENST00000382102.7:c.889-887_889-886del	ENSP00000371534.3:n.889-887_889-886del
ENST00000509381.1:c.563-887_563-886del	ENSP00000421100.1:n.563-887_563-886del
ENST00000510600.1:c.364-887_364-886del	ENSP00000424010.1:n.364-887_364-886del
NM_001012509.3:c.889-887_889-886del	NP_001012527.1:n.889-887_889-886del
NM_001297417.2:c.563-887_563-886del	NP_001284346.2:n.563-887_563-886del
NM_016180.4:c.889-887_889-886del	NP_057264.3:n.889-887_889-886del
XM_011514051.1:c.487-887_487-886del	XP_011512353.1:n.487-887_487-886del
XR_925620.1:n.1706-887_1706-886del
NM_016180.5:c.889-887_889-886del MANE Select	NP_057264.4:n.889-887_889-886del
NM_001012509.4:c.889-887_889-886del	NP_001012527.2:n.889-887_889-886del
NM_001297417.3:c.563-887_563-886del	NP_001284346.2:n.563-887_563-886del
NM_001297417.4:c.563-887_563-886del	NP_001284346.2:n.563-887_563-886del