Canonical Allele Identifier: CA1873825416

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402977_114402978delinsAG , CM000671.2:g.114402977_114402978delinsAG	GRCh38
NC_000009.11:g.117165257_117165258delinsAG , CM000671.1:g.117165257_117165258delinsAG	GRCh37
NC_000009.10:g.116205078_116205079delinsAG	NCBI36
NG_016700.1:g.107479_107480delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.886-42_886-41delinsCT	ENSP00000514396.1:n.886-42_886-41delinsCT
ENST00000362057.4:c.2542-42_2542-41delinsCT MANE Select	ENSP00000354623.3:n.2542-42_2542-41delinsCT
ENST00000674036.8:c.1515-42_1515-41delinsCT
ENST00000674048.1:n.2423-42_2423-41delinsCT
ENST00000265134.10:c.1393-42_1393-41delinsCT	ENSP00000265134.6:n.1393-42_1393-41delinsCT
ENST00000362057.3:c.2542-42_2542-41delinsCT	ENSP00000354623.3:n.2542-42_2542-41delinsCT
ENST00000374059.7:c.1489-42_1489-41delinsCT	ENSP00000363172.3:n.1489-42_1489-41delinsCT
NM_001083885.2:c.1393-42_1393-41delinsCT	NP_001077354.2:n.1393-42_1393-41delinsCT
NM_001173425.1:c.2539-42_2539-41delinsCT	NP_001166896.1:n.2539-42_2539-41delinsCT
NM_015404.3:c.2542-42_2542-41delinsCT	NP_056219.3:n.2542-42_2542-41delinsCT
XM_005251897.3:c.1879-42_1879-41delinsCT	XP_005251954.2:n.1879-42_1879-41delinsCT
XM_011518484.1:c.2575-42_2575-41delinsCT	XP_011516786.1:n.2575-42_2575-41delinsCT
XM_011518485.1:c.2575-42_2575-41delinsCT	XP_011516787.1:n.2575-42_2575-41delinsCT
XM_011518486.1:c.2572-42_2572-41delinsCT	XP_011516788.1:n.2572-42_2572-41delinsCT
XM_011518487.1:c.2449-42_2449-41delinsCT	XP_011516789.1:n.2449-42_2449-41delinsCT
XM_011518488.1:c.2332-42_2332-41delinsCT	XP_011516790.1:n.2332-42_2332-41delinsCT
XM_011518495.1:c.1252-42_1252-41delinsCT	XP_011516797.1:n.1252-42_1252-41delinsCT
XR_929747.1:n.3479-42_3479-41delinsCT
XR_929748.1:n.3377-42_3377-41delinsCT
NM_001346890.1:c.1489-42_1489-41delinsCT	NP_001333819.1:n.1489-42_1489-41delinsCT
XM_011518486.2:c.2572-42_2572-41delinsCT	XP_011516788.1:n.2572-42_2572-41delinsCT
XM_011518487.2:c.2449-42_2449-41delinsCT	XP_011516789.1:n.2449-42_2449-41delinsCT
XM_011518488.2:c.2332-42_2332-41delinsCT	XP_011516790.1:n.2332-42_2332-41delinsCT
XR_929747.2:n.2790-42_2790-41delinsCT
XR_929748.2:n.2688-42_2688-41delinsCT
NM_015404.4:c.2542-42_2542-41delinsCT MANE Select	NP_056219.3:n.2542-42_2542-41delinsCT
NM_001173425.2:c.2539-42_2539-41delinsCT	NP_001166896.1:n.2539-42_2539-41delinsCT
NM_001083885.3:c.1393-42_1393-41delinsCT	NP_001077354.2:n.1393-42_1393-41delinsCT