Canonical Allele Identifier: CA1538189609

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1752352933

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33958761_33958762insAG , CM000667.2:g.33958761_33958762insAG	GRCh38
NC_000005.9:g.33958866_33958867insAG , CM000667.1:g.33958866_33958867insAG	GRCh37
NC_000005.8:g.33994623_33994624insAG	NCBI36
NG_011691.2:g.30914_30915insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-4258_889-4257insCT MANE Select	ENSP00000296589.4:n.889-4258_889-4257insCT
ENST00000296589.8:c.889-4258_889-4257insCT	ENSP00000296589.4:n.889-4258_889-4257insCT
ENST00000382102.7:c.889-4258_889-4257insCT	ENSP00000371534.3:n.889-4258_889-4257insCT
ENST00000509381.1:c.563-4258_563-4257insCT	ENSP00000421100.1:n.563-4258_563-4257insCT
ENST00000510600.1:c.364-4258_364-4257insCT	ENSP00000424010.1:n.364-4258_364-4257insCT
NM_001012509.3:c.889-4258_889-4257insCT	NP_001012527.1:n.889-4258_889-4257insCT
NM_001297417.2:c.563-4258_563-4257insCT	NP_001284346.2:n.563-4258_563-4257insCT
NM_016180.4:c.889-4258_889-4257insCT	NP_057264.3:n.889-4258_889-4257insCT
XM_011514051.1:c.487-4258_487-4257insCT	XP_011512353.1:n.487-4258_487-4257insCT
XR_925620.1:n.1706-4258_1706-4257insCT
NM_016180.5:c.889-4258_889-4257insCT MANE Select	NP_057264.4:n.889-4258_889-4257insCT
NM_001012509.4:c.889-4258_889-4257insCT	NP_001012527.2:n.889-4258_889-4257insCT
NM_001297417.3:c.563-4258_563-4257insCT	NP_001284346.2:n.563-4258_563-4257insCT
NM_001297417.4:c.563-4258_563-4257insCT	NP_001284346.2:n.563-4258_563-4257insCT