Canonical Allele Identifier: CA2765834805
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33964124_33964125del , CM000667.2:g.33964124_33964125del GRCh38
NC_000005.9:g.33964229_33964230del , CM000667.1:g.33964229_33964230del GRCh37
NC_000005.8:g.33999986_33999987del NCBI36
NG_011691.2:g.25551_25552del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.563-109_563-108del MANE Select ENSP00000296589.4:n.563-109_563-108del
ENST00000296589.8:c.563-109_563-108del ENSP00000296589.4:n.563-109_563-108del
ENST00000382102.7:c.563-109_563-108del ENSP00000371534.3:n.563-109_563-108del
ENST00000505056.1:n.365-109_365-108del
ENST00000509381.1:c.563-9621_563-9620del ENSP00000421100.1:n.563-9621_563-9620del
ENST00000510600.1:c.38-109_38-108del ENSP00000424010.1:n.38-109_38-108del
NM_001012509.3:c.563-109_563-108del NP_001012527.1:n.563-109_563-108del
NM_001297417.2:c.563-9621_563-9620del NP_001284346.2:n.563-9621_563-9620del
NM_016180.4:c.563-109_563-108del NP_057264.3:n.563-109_563-108del
XM_011514051.1:c.161-109_161-108del XP_011512353.1:n.161-109_161-108del
XM_011514052.1:c.563-109_563-108del XP_011512354.1:n.563-109_563-108del
XR_925620.1:n.1380-109_1380-108del
NM_016180.5:c.563-109_563-108del MANE Select NP_057264.4:n.563-109_563-108del
NM_001012509.4:c.563-109_563-108del NP_001012527.2:n.563-109_563-108del
NM_001297417.3:c.563-9621_563-9620del NP_001284346.2:n.563-9621_563-9620del
NM_001297417.4:c.563-9621_563-9620del NP_001284346.2:n.563-9621_563-9620del