Canonical Allele Identifier: CA2691372991
Gene: WHRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114407999del , CM000671.2:g.114407999del GRCh38
NC_000009.11:g.117170279del , CM000671.1:g.117170279del GRCh37
NC_000009.10:g.116210100del NCBI36
NG_016700.1:g.102460del

Transcript Alleles

HGVS Amino-acid Change
ENST00000362057.4:c.1648del MANE Select ENSP00000354623.3:p.Thr550LeufsTer?
ENST00000673811.1:n.2372del
ENST00000674036.8:c.621del
ENST00000674048.1:n.1529del
ENST00000265134.10:c.499del ENSP00000265134.6:p.Thr167LeufsTer?
ENST00000362057.3:c.1648del ENSP00000354623.3:p.Thr550LeufsTer?
ENST00000374059.7:c.595del ENSP00000363172.3:p.Thr199LeufsTer?
NM_001083885.2:c.499del NP_001077354.2:p.Thr167LeufsTer?
NM_001173425.1:c.1648del NP_001166896.1:p.Thr550LeufsTer?
NM_015404.3:c.1648del NP_056219.3:p.Thr550LeufsTer?
XM_005251897.3:c.985del XP_005251954.2:p.Thr329LeufsTer?
XM_011518484.1:c.1681del XP_011516786.1:p.Thr561LeufsTer?
XM_011518485.1:c.1681del XP_011516787.1:p.Thr561LeufsTer?
XM_011518486.1:c.1681del XP_011516788.1:p.Thr561LeufsTer?
XM_011518487.1:c.1555del XP_011516789.1:p.Thr519LeufsTer?
XM_011518488.1:c.1438del XP_011516790.1:p.Thr480LeufsTer?
XM_011518492.1:c.*33del XP_011516794.1:n.*33del
XM_011518495.1:c.358del XP_011516797.1:p.Thr120LeufsTer?
XR_929747.1:n.2585del
XR_929748.1:n.2483del
XR_929750.1:n.2584del
XR_929751.1:n.2491del
XR_929757.1:n.2458del
NM_001346890.1:c.595del NP_001333819.1:p.Thr199LeufsTer?
XM_011518486.2:c.1681del XP_011516788.1:p.Thr561LeufsTer?
XM_011518487.2:c.1555del XP_011516789.1:p.Thr519LeufsTer?
XM_011518488.2:c.1438del XP_011516790.1:p.Thr480LeufsTer?
XM_011518492.2:c.*33del XP_011516794.1:n.*33del
XR_929747.2:n.1896del
XR_929748.2:n.1794del
XR_929750.3:n.1895del
XR_929757.2:n.1769del
NM_015404.4:c.1648del MANE Select NP_056219.3:p.Thr550LeufsTer?
NM_001173425.2:c.1648del NP_001166896.1:p.Thr550LeufsTer?
NM_001083885.3:c.499del NP_001077354.2:p.Thr167LeufsTer?