Canonical Allele Identifier: CA916084278

Gene: WHRN

Linked Data

• ClinVar Variation Id: 836299
• ClinVar RCV Id: RCV001037400

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404006_114408890del , CM000671.2:g.114404006_114408890del	GRCh38
NG_016700.1:g.101571_106455del

Transcript Alleles

HGVS	Amino-acid change
ENST00000362057.4:c.1627-868_2312del
ENST00000674036.8:c.600-868_1285del
ENST00000674048.1:n.1508-868_2193del
ENST00000265134.10:c.478-868_1163del
ENST00000362057.3:c.1627-868_2312del
ENST00000374059.7:c.574-868_1259del
NM_001083885.2:c.478-868_1163del
NM_001173425.1:c.1627-868_2309del
NM_015404.3:c.1627-868_2312del
XM_005251897.3:c.964-868_1649del
XM_011518484.1:c.1660-868_2345del
XM_011518485.1:c.1660-868_2345del
XM_011518486.1:c.1660-868_2342del
XM_011518487.1:c.1534-868_2219del
XM_011518488.1:c.1417-868_2102del
XM_011518495.1:c.337-868_1022del
XR_929747.1:n.2564-868_3249del
XR_929748.1:n.2462-868_3147del
NM_001346890.1:c.574-868_1259del
XM_011518486.2:c.1660-868_2342del
XM_011518487.2:c.1534-868_2219del
XM_011518488.2:c.1417-868_2102del
XR_929747.2:n.1875-868_2560del
XR_929748.2:n.1773-868_2458del
NM_015404.4:c.1627-868_2312del
NM_001173425.2:c.1627-868_2309del
NM_001083885.3:c.478-868_1163del