Canonical Allele Identifier: CA2785655997
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114404187_114404188del , CM000671.2:g.114404187_114404188del GRCh38
NC_000009.11:g.117166467_117166468del , CM000671.1:g.117166467_117166468del GRCh37
NC_000009.10:g.116206288_116206289del NCBI36
NG_016700.1:g.106269_106270del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699485.1:c.581-111_581-110del ENSP00000514396.1:n.581-111_581-110del
ENST00000362057.4:c.2237-111_2237-110del MANE Select ENSP00000354623.3:n.2237-111_2237-110del
ENST00000674036.8:c.1210-111_1210-110del
ENST00000674048.1:n.2118-111_2118-110del
ENST00000265134.10:c.1088-111_1088-110del ENSP00000265134.6:n.1088-111_1088-110del
ENST00000362057.3:c.2237-111_2237-110del ENSP00000354623.3:n.2237-111_2237-110del
ENST00000374059.7:c.1184-111_1184-110del ENSP00000363172.3:n.1184-111_1184-110del
NM_001083885.2:c.1088-111_1088-110del NP_001077354.2:n.1088-111_1088-110del
NM_001173425.1:c.2237-114_2237-113del NP_001166896.1:n.2237-114_2237-113del
NM_015404.3:c.2237-111_2237-110del NP_056219.3:n.2237-111_2237-110del
XM_005251897.3:c.1574-111_1574-110del XP_005251954.2:n.1574-111_1574-110del
XM_011518484.1:c.2270-111_2270-110del XP_011516786.1:n.2270-111_2270-110del
XM_011518485.1:c.2270-111_2270-110del XP_011516787.1:n.2270-111_2270-110del
XM_011518486.1:c.2270-114_2270-113del XP_011516788.1:n.2270-114_2270-113del
XM_011518487.1:c.2144-111_2144-110del XP_011516789.1:n.2144-111_2144-110del
XM_011518488.1:c.2027-111_2027-110del XP_011516790.1:n.2027-111_2027-110del
XM_011518495.1:c.947-111_947-110del XP_011516797.1:n.947-111_947-110del
XR_929747.1:n.3174-111_3174-110del
XR_929748.1:n.3072-111_3072-110del
NM_001346890.1:c.1184-111_1184-110del NP_001333819.1:n.1184-111_1184-110del
XM_011518486.2:c.2270-114_2270-113del XP_011516788.1:n.2270-114_2270-113del
XM_011518487.2:c.2144-111_2144-110del XP_011516789.1:n.2144-111_2144-110del
XM_011518488.2:c.2027-111_2027-110del XP_011516790.1:n.2027-111_2027-110del
XR_929747.2:n.2485-111_2485-110del
XR_929748.2:n.2383-111_2383-110del
NM_015404.4:c.2237-111_2237-110del MANE Select NP_056219.3:n.2237-111_2237-110del
NM_001173425.2:c.2237-114_2237-113del NP_001166896.1:n.2237-114_2237-113del
NM_001083885.3:c.1088-111_1088-110del NP_001077354.2:n.1088-111_1088-110del