Canonical Allele Identifier: CA5206191

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114478553del , CM000671.2:g.114478553del	GRCh38
NC_000009.11:g.117240833del , CM000671.1:g.117240833del	GRCh37
NC_000009.10:g.116280654del	NCBI36
NG_016700.1:g.31905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.561+1del
ENST00000362057.4:c.837+1del
ENST00000673811.1:n.585+1del
ENST00000674036.8:c.20+1del
ENST00000265134.10:c.-313+1del
ENST00000362057.3:c.837+1del
ENST00000374057.3:c.838del	ENSP00000363170.3:p.Val280Ter
NM_001083885.2:c.-313+1del
NM_001173425.1:c.837+1del
NM_015404.3:c.837+1del
XM_005251897.3:c.837+1del
XM_011518484.1:c.837+1del
XM_011518485.1:c.837+1del
XM_011518486.1:c.837+1del
XM_011518487.1:c.837+1del
XM_011518488.1:c.837+1del
XM_011518489.1:c.837+1del
XM_011518490.1:c.837+1del
XM_011518491.1:c.837+1del
XM_011518492.1:c.837+1del
XM_011518493.1:c.837+1del
XM_011518494.1:c.837+1del
XR_929747.1:n.1545+1del
XR_929748.1:n.1545+1del
XR_929749.1:n.1545+1del
XR_929750.1:n.1545+1del
XR_929751.1:n.1545+1del
XR_929752.1:n.1545+1del
XR_929753.1:n.1545+1del
XR_929754.1:n.1545+1del
XR_929755.1:n.1545+1del
XR_929756.1:n.1545+1del
XR_929757.1:n.1545+1del
XM_011518486.2:c.837+1del
XM_011518487.2:c.837+1del
XM_011518488.2:c.837+1del
XM_011518489.3:c.837+1del
XM_011518491.3:c.837+1del
XM_011518492.2:c.837+1del
XM_011518494.3:c.837+1del
XR_929747.2:n.856+1del
XR_929748.2:n.856+1del
XR_929749.2:n.856+1del
XR_929750.3:n.856+1del
XR_929752.2:n.856+1del
XR_929753.3:n.856+1del
XR_929754.2:n.856+1del
XR_929755.3:n.856+1del
XR_929756.2:n.856+1del
XR_929757.2:n.856+1del
NM_015404.4:c.837+1del
NM_001173425.2:c.837+1del
NM_001083885.3:c.-313+1del