Canonical Allele Identifier: CA2765834672
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33964071_33964079del , CM000667.2:g.33964071_33964079del GRCh38
NC_000005.9:g.33964176_33964184del , CM000667.1:g.33964176_33964184del GRCh37
NC_000005.8:g.33999933_33999941del NCBI36
NG_011691.2:g.25597_25605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.563-63_563-55del MANE Select ENSP00000296589.4:n.563-63_563-55del
ENST00000296589.8:c.563-63_563-55del ENSP00000296589.4:n.563-63_563-55del
ENST00000382102.7:c.563-63_563-55del ENSP00000371534.3:n.563-63_563-55del
ENST00000505056.1:n.365-63_365-55del
ENST00000509381.1:c.563-9575_563-9567del ENSP00000421100.1:n.563-9575_563-9567del
ENST00000510600.1:c.38-63_38-55del ENSP00000424010.1:n.38-63_38-55del
NM_001012509.3:c.563-63_563-55del NP_001012527.1:n.563-63_563-55del
NM_001297417.2:c.563-9575_563-9567del NP_001284346.2:n.563-9575_563-9567del
NM_016180.4:c.563-63_563-55del NP_057264.3:n.563-63_563-55del
XM_011514051.1:c.161-63_161-55del XP_011512353.1:n.161-63_161-55del
XM_011514052.1:c.563-63_563-55del XP_011512354.1:n.563-63_563-55del
XR_925620.1:n.1380-63_1380-55del
NM_016180.5:c.563-63_563-55del MANE Select NP_057264.4:n.563-63_563-55del
NM_001012509.4:c.563-63_563-55del NP_001012527.2:n.563-63_563-55del
NM_001297417.3:c.563-9575_563-9567del NP_001284346.2:n.563-9575_563-9567del
NM_001297417.4:c.563-9575_563-9567del NP_001284346.2:n.563-9575_563-9567del