Canonical Allele Identifier: CA2785657408

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114424676_114424677insAGT , CM000671.2:g.114424676_114424677insAGT	GRCh38
NC_000009.11:g.117186956_117186957insAGT , CM000671.1:g.117186956_117186957insAGT	GRCh37
NC_000009.10:g.116226777_116226778insAGT	NCBI36
NG_016700.1:g.85780_85781insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.928-131_928-130insACT	ENSP00000514397.1:n.928-131_928-130insACT
ENST00000362057.4:c.1204-131_1204-130insACT MANE Select	ENSP00000354623.3:n.1204-131_1204-130insACT
ENST00000673811.1:n.2138-131_2138-130insACT
ENST00000674036.8:c.387-131_387-130insACT
ENST00000674048.1:n.1085-131_1085-130insACT
ENST00000265134.10:c.55-131_55-130insACT	ENSP00000265134.6:n.55-131_55-130insACT
ENST00000362057.3:c.1204-131_1204-130insACT	ENSP00000354623.3:n.1204-131_1204-130insACT
ENST00000374059.7:c.151-131_151-130insACT	ENSP00000363172.3:n.151-131_151-130insACT
NM_001083885.2:c.55-131_55-130insACT	NP_001077354.2:n.55-131_55-130insACT
NM_001173425.1:c.1204-131_1204-130insACT	NP_001166896.1:n.1204-131_1204-130insACT
NM_015404.3:c.1204-131_1204-130insACT	NP_056219.3:n.1204-131_1204-130insACT
XM_005251897.3:c.964-16659_964-16658insACT	XP_005251954.2:n.964-16659_964-16658insACT
XM_011518484.1:c.1204-131_1204-130insACT	XP_011516786.1:n.1204-131_1204-130insACT
XM_011518485.1:c.1204-131_1204-130insACT	XP_011516787.1:n.1204-131_1204-130insACT
XM_011518486.1:c.1204-131_1204-130insACT	XP_011516788.1:n.1204-131_1204-130insACT
XM_011518487.1:c.1078-131_1078-130insACT	XP_011516789.1:n.1078-131_1078-130insACT
XM_011518488.1:c.1204-131_1204-130insACT	XP_011516790.1:n.1204-131_1204-130insACT
XM_011518489.1:c.1204-131_1204-130insACT	XP_011516791.1:n.1204-131_1204-130insACT
XM_011518490.1:c.1204-131_1204-130insACT	XP_011516792.1:n.1204-131_1204-130insACT
XM_011518491.1:c.1204-131_1204-130insACT	XP_011516793.1:n.1204-131_1204-130insACT
XM_011518492.1:c.1204-131_1204-130insACT	XP_011516794.1:n.1204-131_1204-130insACT
XM_011518493.1:c.1204-131_1204-130insACT	XP_011516795.1:n.1204-131_1204-130insACT
XM_011518494.1:c.1204-131_1204-130insACT	XP_011516796.1:n.1204-131_1204-130insACT
XM_011518495.1:c.-120-131_-120-130insACT	XP_011516797.1:n.-120-131_-120-130insACT
XR_929747.1:n.1912-131_1912-130insACT
XR_929748.1:n.1912-131_1912-130insACT
XR_929749.1:n.1912-131_1912-130insACT
XR_929750.1:n.1912-131_1912-130insACT
XR_929751.1:n.1912-131_1912-130insACT
XR_929752.1:n.1912-131_1912-130insACT
XR_929753.1:n.1912-131_1912-130insACT
XR_929754.1:n.1912-131_1912-130insACT
XR_929755.1:n.1912-131_1912-130insACT
XR_929756.1:n.1912-131_1912-130insACT
XR_929757.1:n.1912-131_1912-130insACT
NM_001346890.1:c.151-131_151-130insACT	NP_001333819.1:n.151-131_151-130insACT
XM_011518486.2:c.1204-131_1204-130insACT	XP_011516788.1:n.1204-131_1204-130insACT
XM_011518487.2:c.1078-131_1078-130insACT	XP_011516789.1:n.1078-131_1078-130insACT
XM_011518488.2:c.1204-131_1204-130insACT	XP_011516790.1:n.1204-131_1204-130insACT
XM_011518489.3:c.1204-131_1204-130insACT	XP_011516791.1:n.1204-131_1204-130insACT
XM_011518491.3:c.1204-131_1204-130insACT	XP_011516793.1:n.1204-131_1204-130insACT
XM_011518492.2:c.1204-131_1204-130insACT	XP_011516794.1:n.1204-131_1204-130insACT
XM_011518494.3:c.1204-131_1204-130insACT	XP_011516796.1:n.1204-131_1204-130insACT
XR_929747.2:n.1223-131_1223-130insACT
XR_929748.2:n.1223-131_1223-130insACT
XR_929749.2:n.1223-131_1223-130insACT
XR_929750.3:n.1223-131_1223-130insACT
XR_929752.2:n.1223-131_1223-130insACT
XR_929753.3:n.1223-131_1223-130insACT
XR_929754.2:n.1223-131_1223-130insACT
XR_929755.3:n.1223-131_1223-130insACT
XR_929756.2:n.1223-131_1223-130insACT
XR_929757.2:n.1223-131_1223-130insACT
NM_015404.4:c.1204-131_1204-130insACT MANE Select	NP_056219.3:n.1204-131_1204-130insACT
NM_001173425.2:c.1204-131_1204-130insACT	NP_001166896.1:n.1204-131_1204-130insACT
NM_001083885.3:c.55-131_55-130insACT	NP_001077354.2:n.55-131_55-130insACT