Canonical Allele Identifier: CA2691372454
Gene: WHRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114404185_114404186insTCTTTGCCTGG , CM000671.2:g.114404185_114404186insTCTTTGCCTGG GRCh38
NC_000009.11:g.117166465_117166466insTCTTTGCCTGG , CM000671.1:g.117166465_117166466insTCTTTGCCTGG GRCh37
NC_000009.10:g.116206286_116206287insTCTTTGCCTGG NCBI36
NG_016700.1:g.106271_106272insCCAGGCAAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000699485.1:c.581-109_581-108insCCAGGCAAAGA ENSP00000514396.1:n.581-109_581-108insCCAGGCAAAGA
ENST00000362057.4:c.2237-109_2237-108insCCAGGCAAAGA MANE Select ENSP00000354623.3:n.2237-109_2237-108insCCAGGCAAAGA
ENST00000674036.8:c.1210-109_1210-108insCCAGGCAAAGA
ENST00000674048.1:n.2118-109_2118-108insCCAGGCAAAGA
ENST00000265134.10:c.1088-109_1088-108insCCAGGCAAAGA ENSP00000265134.6:n.1088-109_1088-108insCCAGGCAAAGA
ENST00000362057.3:c.2237-109_2237-108insCCAGGCAAAGA ENSP00000354623.3:n.2237-109_2237-108insCCAGGCAAAGA
ENST00000374059.7:c.1184-109_1184-108insCCAGGCAAAGA ENSP00000363172.3:n.1184-109_1184-108insCCAGGCAAAGA
NM_001083885.2:c.1088-109_1088-108insCCAGGCAAAGA NP_001077354.2:n.1088-109_1088-108insCCAGGCAAAGA
NM_001173425.1:c.2237-112_2237-111insCCAGGCAAAGA NP_001166896.1:n.2237-112_2237-111insCCAGGCAAAGA
NM_015404.3:c.2237-109_2237-108insCCAGGCAAAGA NP_056219.3:n.2237-109_2237-108insCCAGGCAAAGA
XM_005251897.3:c.1574-109_1574-108insCCAGGCAAAGA XP_005251954.2:n.1574-109_1574-108insCCAGGCAAAGA
XM_011518484.1:c.2270-109_2270-108insCCAGGCAAAGA XP_011516786.1:n.2270-109_2270-108insCCAGGCAAAGA
XM_011518485.1:c.2270-109_2270-108insCCAGGCAAAGA XP_011516787.1:n.2270-109_2270-108insCCAGGCAAAGA
XM_011518486.1:c.2270-112_2270-111insCCAGGCAAAGA XP_011516788.1:n.2270-112_2270-111insCCAGGCAAAGA
XM_011518487.1:c.2144-109_2144-108insCCAGGCAAAGA XP_011516789.1:n.2144-109_2144-108insCCAGGCAAAGA
XM_011518488.1:c.2027-109_2027-108insCCAGGCAAAGA XP_011516790.1:n.2027-109_2027-108insCCAGGCAAAGA
XM_011518495.1:c.947-109_947-108insCCAGGCAAAGA XP_011516797.1:n.947-109_947-108insCCAGGCAAAGA
XR_929747.1:n.3174-109_3174-108insCCAGGCAAAGA
XR_929748.1:n.3072-109_3072-108insCCAGGCAAAGA
NM_001346890.1:c.1184-109_1184-108insCCAGGCAAAGA NP_001333819.1:n.1184-109_1184-108insCCAGGCAAAGA
XM_011518486.2:c.2270-112_2270-111insCCAGGCAAAGA XP_011516788.1:n.2270-112_2270-111insCCAGGCAAAGA
XM_011518487.2:c.2144-109_2144-108insCCAGGCAAAGA XP_011516789.1:n.2144-109_2144-108insCCAGGCAAAGA
XM_011518488.2:c.2027-109_2027-108insCCAGGCAAAGA XP_011516790.1:n.2027-109_2027-108insCCAGGCAAAGA
XR_929747.2:n.2485-109_2485-108insCCAGGCAAAGA
XR_929748.2:n.2383-109_2383-108insCCAGGCAAAGA
NM_015404.4:c.2237-109_2237-108insCCAGGCAAAGA MANE Select NP_056219.3:n.2237-109_2237-108insCCAGGCAAAGA
NM_001173425.2:c.2237-112_2237-111insCCAGGCAAAGA NP_001166896.1:n.2237-112_2237-111insCCAGGCAAAGA
NM_001083885.3:c.1088-109_1088-108insCCAGGCAAAGA NP_001077354.2:n.1088-109_1088-108insCCAGGCAAAGA