Canonical Allele Identifier: CA2579434571
Gene: WHRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114402998_114403000del , CM000671.2:g.114402998_114403000del GRCh38
NC_000009.11:g.117165278_117165280del , CM000671.1:g.117165278_117165280del GRCh37
NC_000009.10:g.116205099_116205101del NCBI36
NG_016700.1:g.107461_107463del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699485.1:c.886-60_886-58del ENSP00000514396.1:n.886-60_886-58del
ENST00000362057.4:c.2542-60_2542-58del MANE Select ENSP00000354623.3:n.2542-60_2542-58del
ENST00000674036.8:c.1515-60_1515-58del
ENST00000674048.1:n.2423-60_2423-58del
ENST00000265134.10:c.1393-60_1393-58del ENSP00000265134.6:n.1393-60_1393-58del
ENST00000362057.3:c.2542-60_2542-58del ENSP00000354623.3:n.2542-60_2542-58del
ENST00000374059.7:c.1489-60_1489-58del ENSP00000363172.3:n.1489-60_1489-58del
NM_001083885.2:c.1393-60_1393-58del NP_001077354.2:n.1393-60_1393-58del
NM_001173425.1:c.2539-60_2539-58del NP_001166896.1:n.2539-60_2539-58del
NM_015404.3:c.2542-60_2542-58del NP_056219.3:n.2542-60_2542-58del
XM_005251897.3:c.1879-60_1879-58del XP_005251954.2:n.1879-60_1879-58del
XM_011518484.1:c.2575-60_2575-58del XP_011516786.1:n.2575-60_2575-58del
XM_011518485.1:c.2575-60_2575-58del XP_011516787.1:n.2575-60_2575-58del
XM_011518486.1:c.2572-60_2572-58del XP_011516788.1:n.2572-60_2572-58del
XM_011518487.1:c.2449-60_2449-58del XP_011516789.1:n.2449-60_2449-58del
XM_011518488.1:c.2332-60_2332-58del XP_011516790.1:n.2332-60_2332-58del
XM_011518495.1:c.1252-60_1252-58del XP_011516797.1:n.1252-60_1252-58del
XR_929747.1:n.3479-60_3479-58del
XR_929748.1:n.3377-60_3377-58del
NM_001346890.1:c.1489-60_1489-58del NP_001333819.1:n.1489-60_1489-58del
XM_011518486.2:c.2572-60_2572-58del XP_011516788.1:n.2572-60_2572-58del
XM_011518487.2:c.2449-60_2449-58del XP_011516789.1:n.2449-60_2449-58del
XM_011518488.2:c.2332-60_2332-58del XP_011516790.1:n.2332-60_2332-58del
XR_929747.2:n.2790-60_2790-58del
XR_929748.2:n.2688-60_2688-58del
NM_015404.4:c.2542-60_2542-58del MANE Select NP_056219.3:n.2542-60_2542-58del
NM_001173425.2:c.2539-60_2539-58del NP_001166896.1:n.2539-60_2539-58del
NM_001083885.3:c.1393-60_1393-58del NP_001077354.2:n.1393-60_1393-58del