Canonical Allele Identifier: CA2785655552

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403057_114403093del , CM000671.2:g.114403057_114403093del	GRCh38
NC_000009.11:g.117165337_117165373del , CM000671.1:g.117165337_117165373del	GRCh37
NC_000009.10:g.116205158_116205194del	NCBI36
NG_016700.1:g.107364_107400del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.885+124_886-121del	ENSP00000514396.1:n.885+124_886-121del
ENST00000362057.4:c.2541+124_2542-121del MANE Select	ENSP00000354623.3:n.2541+124_2542-121del
ENST00000674036.8:c.1514+124_1515-121del
ENST00000674048.1:n.2422+124_2423-121del
ENST00000265134.10:c.1392+124_1393-121del	ENSP00000265134.6:n.1392+124_1393-121del
ENST00000362057.3:c.2541+124_2542-121del	ENSP00000354623.3:n.2541+124_2542-121del
ENST00000374059.7:c.1488+124_1489-121del	ENSP00000363172.3:n.1488+124_1489-121del
NM_001083885.2:c.1392+124_1393-121del	NP_001077354.2:n.1392+124_1393-121del
NM_001173425.1:c.2538+124_2539-121del	NP_001166896.1:n.2538+124_2539-121del
NM_015404.3:c.2541+124_2542-121del	NP_056219.3:n.2541+124_2542-121del
XM_005251897.3:c.1878+124_1879-121del	XP_005251954.2:n.1878+124_1879-121del
XM_011518484.1:c.2574+124_2575-121del	XP_011516786.1:n.2574+124_2575-121del
XM_011518485.1:c.2574+124_2575-121del	XP_011516787.1:n.2574+124_2575-121del
XM_011518486.1:c.2571+124_2572-121del	XP_011516788.1:n.2571+124_2572-121del
XM_011518487.1:c.2448+124_2449-121del	XP_011516789.1:n.2448+124_2449-121del
XM_011518488.1:c.2331+124_2332-121del	XP_011516790.1:n.2331+124_2332-121del
XM_011518495.1:c.1251+124_1252-121del	XP_011516797.1:n.1251+124_1252-121del
XR_929747.1:n.3478+124_3479-121del
XR_929748.1:n.3376+124_3377-121del
NM_001346890.1:c.1488+124_1489-121del	NP_001333819.1:n.1488+124_1489-121del
XM_011518486.2:c.2571+124_2572-121del	XP_011516788.1:n.2571+124_2572-121del
XM_011518487.2:c.2448+124_2449-121del	XP_011516789.1:n.2448+124_2449-121del
XM_011518488.2:c.2331+124_2332-121del	XP_011516790.1:n.2331+124_2332-121del
XR_929747.2:n.2789+124_2790-121del
XR_929748.2:n.2687+124_2688-121del
NM_015404.4:c.2541+124_2542-121del MANE Select	NP_056219.3:n.2541+124_2542-121del
NM_001173425.2:c.2538+124_2539-121del	NP_001166896.1:n.2538+124_2539-121del
NM_001083885.3:c.1392+124_1393-121del	NP_001077354.2:n.1392+124_1393-121del