Canonical Allele Identifier: CA2785655544

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403034_114403035insACG , CM000671.2:g.114403034_114403035insACG	GRCh38
NC_000009.11:g.117165314_117165315insACG , CM000671.1:g.117165314_117165315insACG	GRCh37
NC_000009.10:g.116205135_116205136insACG	NCBI36
NG_016700.1:g.107422_107423insCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.886-99_886-98insCGT	ENSP00000514396.1:n.886-99_886-98insCGT
ENST00000362057.4:c.2542-99_2542-98insCGT MANE Select	ENSP00000354623.3:n.2542-99_2542-98insCGT
ENST00000674036.8:c.1515-99_1515-98insCGT
ENST00000674048.1:n.2423-99_2423-98insCGT
ENST00000265134.10:c.1393-99_1393-98insCGT	ENSP00000265134.6:n.1393-99_1393-98insCGT
ENST00000362057.3:c.2542-99_2542-98insCGT	ENSP00000354623.3:n.2542-99_2542-98insCGT
ENST00000374059.7:c.1489-99_1489-98insCGT	ENSP00000363172.3:n.1489-99_1489-98insCGT
NM_001083885.2:c.1393-99_1393-98insCGT	NP_001077354.2:n.1393-99_1393-98insCGT
NM_001173425.1:c.2539-99_2539-98insCGT	NP_001166896.1:n.2539-99_2539-98insCGT
NM_015404.3:c.2542-99_2542-98insCGT	NP_056219.3:n.2542-99_2542-98insCGT
XM_005251897.3:c.1879-99_1879-98insCGT	XP_005251954.2:n.1879-99_1879-98insCGT
XM_011518484.1:c.2575-99_2575-98insCGT	XP_011516786.1:n.2575-99_2575-98insCGT
XM_011518485.1:c.2575-99_2575-98insCGT	XP_011516787.1:n.2575-99_2575-98insCGT
XM_011518486.1:c.2572-99_2572-98insCGT	XP_011516788.1:n.2572-99_2572-98insCGT
XM_011518487.1:c.2449-99_2449-98insCGT	XP_011516789.1:n.2449-99_2449-98insCGT
XM_011518488.1:c.2332-99_2332-98insCGT	XP_011516790.1:n.2332-99_2332-98insCGT
XM_011518495.1:c.1252-99_1252-98insCGT	XP_011516797.1:n.1252-99_1252-98insCGT
XR_929747.1:n.3479-99_3479-98insCGT
XR_929748.1:n.3377-99_3377-98insCGT
NM_001346890.1:c.1489-99_1489-98insCGT	NP_001333819.1:n.1489-99_1489-98insCGT
XM_011518486.2:c.2572-99_2572-98insCGT	XP_011516788.1:n.2572-99_2572-98insCGT
XM_011518487.2:c.2449-99_2449-98insCGT	XP_011516789.1:n.2449-99_2449-98insCGT
XM_011518488.2:c.2332-99_2332-98insCGT	XP_011516790.1:n.2332-99_2332-98insCGT
XR_929747.2:n.2790-99_2790-98insCGT
XR_929748.2:n.2688-99_2688-98insCGT
NM_015404.4:c.2542-99_2542-98insCGT MANE Select	NP_056219.3:n.2542-99_2542-98insCGT
NM_001173425.2:c.2539-99_2539-98insCGT	NP_001166896.1:n.2539-99_2539-98insCGT
NM_001083885.3:c.1393-99_1393-98insCGT	NP_001077354.2:n.1393-99_1393-98insCGT