Canonical Allele Identifier: CA2691374868

Gene: WHRN

Linked Data

• gnomAD v4: 9-114478357-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114478359_114478360del , CM000671.2:g.114478359_114478360del	GRCh38
NC_000009.11:g.117240639_117240640del , CM000671.1:g.117240639_117240640del	GRCh37
NC_000009.10:g.116280460_116280461del	NCBI36
NG_016700.1:g.32098_32099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.561+194_561+195del	ENSP00000514397.1:n.561+194_561+195del
ENST00000362057.4:c.837+194_837+195del MANE Select	ENSP00000354623.3:n.837+194_837+195del
ENST00000673811.1:n.585+194_585+195del
ENST00000674036.8:c.20+194_20+195del
ENST00000265134.10:c.-313+194_-313+195del	ENSP00000265134.6:n.-313+194_-313+195del
ENST00000362057.3:c.837+194_837+195del	ENSP00000354623.3:n.837+194_837+195del
ENST00000374057.3:c.1031_1032del	ENSP00000363170.3:p.Thr344ArgfsTer10
NM_001083885.2:c.-313+194_-313+195del	NP_001077354.2:n.-313+194_-313+195del
NM_001173425.1:c.837+194_837+195del	NP_001166896.1:n.837+194_837+195del
NM_015404.3:c.837+194_837+195del	NP_056219.3:n.837+194_837+195del
XM_005251897.3:c.837+194_837+195del	XP_005251954.2:n.837+194_837+195del
XM_011518484.1:c.837+194_837+195del	XP_011516786.1:n.837+194_837+195del
XM_011518485.1:c.837+194_837+195del	XP_011516787.1:n.837+194_837+195del
XM_011518486.1:c.837+194_837+195del	XP_011516788.1:n.837+194_837+195del
XM_011518487.1:c.837+194_837+195del	XP_011516789.1:n.837+194_837+195del
XM_011518488.1:c.837+194_837+195del	XP_011516790.1:n.837+194_837+195del
XM_011518489.1:c.837+194_837+195del	XP_011516791.1:n.837+194_837+195del
XM_011518490.1:c.837+194_837+195del	XP_011516792.1:n.837+194_837+195del
XM_011518491.1:c.837+194_837+195del	XP_011516793.1:n.837+194_837+195del
XM_011518492.1:c.837+194_837+195del	XP_011516794.1:n.837+194_837+195del
XM_011518493.1:c.837+194_837+195del	XP_011516795.1:n.837+194_837+195del
XM_011518494.1:c.837+194_837+195del	XP_011516796.1:n.837+194_837+195del
XR_929747.1:n.1545+194_1545+195del
XR_929748.1:n.1545+194_1545+195del
XR_929749.1:n.1545+194_1545+195del
XR_929750.1:n.1545+194_1545+195del
XR_929751.1:n.1545+194_1545+195del
XR_929752.1:n.1545+194_1545+195del
XR_929753.1:n.1545+194_1545+195del
XR_929754.1:n.1545+194_1545+195del
XR_929755.1:n.1545+194_1545+195del
XR_929756.1:n.1545+194_1545+195del
XR_929757.1:n.1545+194_1545+195del
XM_011518486.2:c.837+194_837+195del	XP_011516788.1:n.837+194_837+195del
XM_011518487.2:c.837+194_837+195del	XP_011516789.1:n.837+194_837+195del
XM_011518488.2:c.837+194_837+195del	XP_011516790.1:n.837+194_837+195del
XM_011518489.3:c.837+194_837+195del	XP_011516791.1:n.837+194_837+195del
XM_011518491.3:c.837+194_837+195del	XP_011516793.1:n.837+194_837+195del
XM_011518492.2:c.837+194_837+195del	XP_011516794.1:n.837+194_837+195del
XM_011518494.3:c.837+194_837+195del	XP_011516796.1:n.837+194_837+195del
XR_929747.2:n.856+194_856+195del
XR_929748.2:n.856+194_856+195del
XR_929749.2:n.856+194_856+195del
XR_929750.3:n.856+194_856+195del
XR_929752.2:n.856+194_856+195del
XR_929753.3:n.856+194_856+195del
XR_929754.2:n.856+194_856+195del
XR_929755.3:n.856+194_856+195del
XR_929756.2:n.856+194_856+195del
XR_929757.2:n.856+194_856+195del
NM_015404.4:c.837+194_837+195del MANE Select	NP_056219.3:n.837+194_837+195del
NM_001173425.2:c.837+194_837+195del	NP_001166896.1:n.837+194_837+195del
NM_001083885.3:c.-313+194_-313+195del	NP_001077354.2:n.-313+194_-313+195del