Canonical Allele Identifier: CA2785655549
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114403047_114403048insAGTA , CM000671.2:g.114403047_114403048insAGTA GRCh38
NC_000009.11:g.117165327_117165328insAGTA , CM000671.1:g.117165327_117165328insAGTA GRCh37
NC_000009.10:g.116205148_116205149insAGTA NCBI36
NG_016700.1:g.107409_107410insTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000699485.1:c.886-112_886-111insTACT ENSP00000514396.1:n.886-112_886-111insTACT
ENST00000362057.4:c.2542-112_2542-111insTACT MANE Select ENSP00000354623.3:n.2542-112_2542-111insTACT
ENST00000674036.8:c.1515-112_1515-111insTACT
ENST00000674048.1:n.2423-112_2423-111insTACT
ENST00000265134.10:c.1393-112_1393-111insTACT ENSP00000265134.6:n.1393-112_1393-111insTACT
ENST00000362057.3:c.2542-112_2542-111insTACT ENSP00000354623.3:n.2542-112_2542-111insTACT
ENST00000374059.7:c.1489-112_1489-111insTACT ENSP00000363172.3:n.1489-112_1489-111insTACT
NM_001083885.2:c.1393-112_1393-111insTACT NP_001077354.2:n.1393-112_1393-111insTACT
NM_001173425.1:c.2539-112_2539-111insTACT NP_001166896.1:n.2539-112_2539-111insTACT
NM_015404.3:c.2542-112_2542-111insTACT NP_056219.3:n.2542-112_2542-111insTACT
XM_005251897.3:c.1879-112_1879-111insTACT XP_005251954.2:n.1879-112_1879-111insTACT
XM_011518484.1:c.2575-112_2575-111insTACT XP_011516786.1:n.2575-112_2575-111insTACT
XM_011518485.1:c.2575-112_2575-111insTACT XP_011516787.1:n.2575-112_2575-111insTACT
XM_011518486.1:c.2572-112_2572-111insTACT XP_011516788.1:n.2572-112_2572-111insTACT
XM_011518487.1:c.2449-112_2449-111insTACT XP_011516789.1:n.2449-112_2449-111insTACT
XM_011518488.1:c.2332-112_2332-111insTACT XP_011516790.1:n.2332-112_2332-111insTACT
XM_011518495.1:c.1252-112_1252-111insTACT XP_011516797.1:n.1252-112_1252-111insTACT
XR_929747.1:n.3479-112_3479-111insTACT
XR_929748.1:n.3377-112_3377-111insTACT
NM_001346890.1:c.1489-112_1489-111insTACT NP_001333819.1:n.1489-112_1489-111insTACT
XM_011518486.2:c.2572-112_2572-111insTACT XP_011516788.1:n.2572-112_2572-111insTACT
XM_011518487.2:c.2449-112_2449-111insTACT XP_011516789.1:n.2449-112_2449-111insTACT
XM_011518488.2:c.2332-112_2332-111insTACT XP_011516790.1:n.2332-112_2332-111insTACT
XR_929747.2:n.2790-112_2790-111insTACT
XR_929748.2:n.2688-112_2688-111insTACT
NM_015404.4:c.2542-112_2542-111insTACT MANE Select NP_056219.3:n.2542-112_2542-111insTACT
NM_001173425.2:c.2539-112_2539-111insTACT NP_001166896.1:n.2539-112_2539-111insTACT
NM_001083885.3:c.1393-112_1393-111insTACT NP_001077354.2:n.1393-112_1393-111insTACT