Canonical Allele Identifier: CA2725068213
Gene: HYOU1 HGNC NCBI

Linked Data

dbSNP Id: rs2134697713

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119052868_119052869del , CM000673.2:g.119052868_119052869del GRCh38
NC_000011.8:g.118428790_118428791del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527038.7:c.795-37_795-36del ENSP00000463742.3:n.795-37_795-36del
ENST00000530467.6:c.795-37_795-36del ENSP00000479845.2:n.795-37_795-36del
ENST00000530473.6:c.795-37_795-36del ENSP00000431874.2:n.795-37_795-36del
ENST00000532421.6:c.795-37_795-36del ENSP00000463515.2:n.795-37_795-36del
ENST00000532519.7:c.795-37_795-36del ENSP00000467866.3:n.795-37_795-36del
ENST00000533381.6:n.1032-37_1032-36del
ENST00000534233.6:c.795-37_795-36del ENSP00000462951.2:n.795-37_795-36del
ENST00000610597.2:c.795-37_795-36del ENSP00000484622.2:n.795-37_795-36del
ENST00000614711.5:c.795-37_795-36del ENSP00000480248.2:n.795-37_795-36del
ENST00000694929.1:n.1349-37_1349-36del
ENST00000694930.1:n.985-37_985-36del
ENST00000694932.1:c.795-37_795-36del ENSP00000511598.1:n.795-37_795-36del
ENST00000694933.1:c.795-37_795-36del ENSP00000511599.1:n.795-37_795-36del
ENST00000694934.1:c.795-37_795-36del ENSP00000511600.1:n.795-37_795-36del
ENST00000694935.1:c.795-37_795-36del ENSP00000511601.1:n.795-37_795-36del
ENST00000694937.1:c.*314-37_*314-36del ENSP00000511603.1:n.*314-37_*314-36del
ENST00000617285.5:c.795-37_795-36del MANE Select ENSP00000480150.1:n.795-37_795-36del
ENST00000652093.1:c.795-37_795-36del ENSP00000498353.1:n.795-37_795-36del
ENST00000530473.5:c.795-37_795-36del ENSP00000431874.1:n.795-37_795-36del
ENST00000531694.5:n.1864_1865del
ENST00000532519.6:c.795-37_795-36del ENSP00000467866.2:n.795-37_795-36del
ENST00000543287.5:c.*584-37_*584-36del ENSP00000442727.2:n.*584-37_*584-36del
ENST00000612687.4:c.795-37_795-36del ENSP00000483106.1:n.795-37_795-36del
ENST00000614668.4:c.436+2178_436+2179del ENSP00000482199.1:n.436+2178_436+2179del
ENST00000614711.4:c.795-37_795-36del ENSP00000480248.1:n.795-37_795-36del
ENST00000617285.4:c.795-37_795-36del ENSP00000480150.1:n.795-37_795-36del
ENST00000621959.4:c.795-37_795-36del ENSP00000484186.1:n.795-37_795-36del
NM_001130991.2:c.795-37_795-36del NP_001124463.1:n.795-37_795-36del
NM_006389.4:c.795-37_795-36del NP_006380.1:n.795-37_795-36del
XM_005271392.2:c.795-37_795-36del XP_005271449.1:n.795-37_795-36del
XM_005271393.2:c.795-37_795-36del XP_005271450.1:n.795-37_795-36del
XM_005271394.2:c.795-37_795-36del XP_005271451.1:n.795-37_795-36del
XM_011542557.1:c.927-37_927-36del XP_011540859.1:n.927-37_927-36del
XM_011542558.1:c.927-37_927-36del XP_011540860.1:n.927-37_927-36del
XR_947790.1:n.942-37_942-36del
XM_005271392.4:c.795-37_795-36del XP_005271449.1:n.795-37_795-36del
XM_005271393.3:c.795-37_795-36del XP_005271450.1:n.795-37_795-36del
XM_005271394.3:c.795-37_795-36del XP_005271451.1:n.795-37_795-36del
XM_017017095.1:c.795-37_795-36del XP_016872584.1:n.795-37_795-36del
XM_017017096.1:c.795-37_795-36del XP_016872585.1:n.795-37_795-36del
XM_017017097.1:c.795-37_795-36del XP_016872586.1:n.795-37_795-36del
XR_001747729.1:n.925-37_925-36del
XR_002957117.1:n.925-37_925-36del
NM_006389.5:c.795-37_795-36del MANE Select NP_006380.1:n.795-37_795-36del
NM_001130991.3:c.795-37_795-36del NP_001124463.1:n.795-37_795-36del