Canonical Allele Identifier: CA2765834791
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33964106_33964108del , CM000667.2:g.33964106_33964108del GRCh38
NC_000005.9:g.33964211_33964213del , CM000667.1:g.33964211_33964213del GRCh37
NC_000005.8:g.33999968_33999970del NCBI36
NG_011691.2:g.25568_25570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.563-92_563-90del MANE Select ENSP00000296589.4:n.563-92_563-90del
ENST00000296589.8:c.563-92_563-90del ENSP00000296589.4:n.563-92_563-90del
ENST00000382102.7:c.563-92_563-90del ENSP00000371534.3:n.563-92_563-90del
ENST00000505056.1:n.365-92_365-90del
ENST00000509381.1:c.563-9604_563-9602del ENSP00000421100.1:n.563-9604_563-9602del
ENST00000510600.1:c.38-92_38-90del ENSP00000424010.1:n.38-92_38-90del
NM_001012509.3:c.563-92_563-90del NP_001012527.1:n.563-92_563-90del
NM_001297417.2:c.563-9604_563-9602del NP_001284346.2:n.563-9604_563-9602del
NM_016180.4:c.563-92_563-90del NP_057264.3:n.563-92_563-90del
XM_011514051.1:c.161-92_161-90del XP_011512353.1:n.161-92_161-90del
XM_011514052.1:c.563-92_563-90del XP_011512354.1:n.563-92_563-90del
XR_925620.1:n.1380-92_1380-90del
NM_016180.5:c.563-92_563-90del MANE Select NP_057264.4:n.563-92_563-90del
NM_001012509.4:c.563-92_563-90del NP_001012527.2:n.563-92_563-90del
NM_001297417.3:c.563-9604_563-9602del NP_001284346.2:n.563-9604_563-9602del
NM_001297417.4:c.563-9604_563-9602del NP_001284346.2:n.563-9604_563-9602del