Canonical Allele Identifier: CA2785657307

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114424579_114424580insAG , CM000671.2:g.114424579_114424580insAG	GRCh38
NC_000009.11:g.117186859_117186860insAG , CM000671.1:g.117186859_117186860insAG	GRCh37
NC_000009.10:g.116226680_116226681insAG	NCBI36
NG_016700.1:g.85877_85878insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.928-34_928-33insCT	ENSP00000514397.1:n.928-34_928-33insCT
ENST00000362057.4:c.1204-34_1204-33insCT MANE Select	ENSP00000354623.3:n.1204-34_1204-33insCT
ENST00000673811.1:n.2138-34_2138-33insCT
ENST00000674036.8:c.387-34_387-33insCT
ENST00000674048.1:n.1085-34_1085-33insCT
ENST00000265134.10:c.55-34_55-33insCT	ENSP00000265134.6:n.55-34_55-33insCT
ENST00000362057.3:c.1204-34_1204-33insCT	ENSP00000354623.3:n.1204-34_1204-33insCT
ENST00000374059.7:c.151-34_151-33insCT	ENSP00000363172.3:n.151-34_151-33insCT
NM_001083885.2:c.55-34_55-33insCT	NP_001077354.2:n.55-34_55-33insCT
NM_001173425.1:c.1204-34_1204-33insCT	NP_001166896.1:n.1204-34_1204-33insCT
NM_015404.3:c.1204-34_1204-33insCT	NP_056219.3:n.1204-34_1204-33insCT
XM_005251897.3:c.964-16562_964-16561insCT	XP_005251954.2:n.964-16562_964-16561insCT
XM_011518484.1:c.1204-34_1204-33insCT	XP_011516786.1:n.1204-34_1204-33insCT
XM_011518485.1:c.1204-34_1204-33insCT	XP_011516787.1:n.1204-34_1204-33insCT
XM_011518486.1:c.1204-34_1204-33insCT	XP_011516788.1:n.1204-34_1204-33insCT
XM_011518487.1:c.1078-34_1078-33insCT	XP_011516789.1:n.1078-34_1078-33insCT
XM_011518488.1:c.1204-34_1204-33insCT	XP_011516790.1:n.1204-34_1204-33insCT
XM_011518489.1:c.1204-34_1204-33insCT	XP_011516791.1:n.1204-34_1204-33insCT
XM_011518490.1:c.1204-34_1204-33insCT	XP_011516792.1:n.1204-34_1204-33insCT
XM_011518491.1:c.1204-34_1204-33insCT	XP_011516793.1:n.1204-34_1204-33insCT
XM_011518492.1:c.1204-34_1204-33insCT	XP_011516794.1:n.1204-34_1204-33insCT
XM_011518493.1:c.1204-34_1204-33insCT	XP_011516795.1:n.1204-34_1204-33insCT
XM_011518494.1:c.1204-34_1204-33insCT	XP_011516796.1:n.1204-34_1204-33insCT
XM_011518495.1:c.-120-34_-120-33insCT	XP_011516797.1:n.-120-34_-120-33insCT
XR_929747.1:n.1912-34_1912-33insCT
XR_929748.1:n.1912-34_1912-33insCT
XR_929749.1:n.1912-34_1912-33insCT
XR_929750.1:n.1912-34_1912-33insCT
XR_929751.1:n.1912-34_1912-33insCT
XR_929752.1:n.1912-34_1912-33insCT
XR_929753.1:n.1912-34_1912-33insCT
XR_929754.1:n.1912-34_1912-33insCT
XR_929755.1:n.1912-34_1912-33insCT
XR_929756.1:n.1912-34_1912-33insCT
XR_929757.1:n.1912-34_1912-33insCT
NM_001346890.1:c.151-34_151-33insCT	NP_001333819.1:n.151-34_151-33insCT
XM_011518486.2:c.1204-34_1204-33insCT	XP_011516788.1:n.1204-34_1204-33insCT
XM_011518487.2:c.1078-34_1078-33insCT	XP_011516789.1:n.1078-34_1078-33insCT
XM_011518488.2:c.1204-34_1204-33insCT	XP_011516790.1:n.1204-34_1204-33insCT
XM_011518489.3:c.1204-34_1204-33insCT	XP_011516791.1:n.1204-34_1204-33insCT
XM_011518491.3:c.1204-34_1204-33insCT	XP_011516793.1:n.1204-34_1204-33insCT
XM_011518492.2:c.1204-34_1204-33insCT	XP_011516794.1:n.1204-34_1204-33insCT
XM_011518494.3:c.1204-34_1204-33insCT	XP_011516796.1:n.1204-34_1204-33insCT
XR_929747.2:n.1223-34_1223-33insCT
XR_929748.2:n.1223-34_1223-33insCT
XR_929749.2:n.1223-34_1223-33insCT
XR_929750.3:n.1223-34_1223-33insCT
XR_929752.2:n.1223-34_1223-33insCT
XR_929753.3:n.1223-34_1223-33insCT
XR_929754.2:n.1223-34_1223-33insCT
XR_929755.3:n.1223-34_1223-33insCT
XR_929756.2:n.1223-34_1223-33insCT
XR_929757.2:n.1223-34_1223-33insCT
NM_015404.4:c.1204-34_1204-33insCT MANE Select	NP_056219.3:n.1204-34_1204-33insCT
NM_001173425.2:c.1204-34_1204-33insCT	NP_001166896.1:n.1204-34_1204-33insCT
NM_001083885.3:c.55-34_55-33insCT	NP_001077354.2:n.55-34_55-33insCT