Canonical Allele Identifier: CA2785655509

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402985_114402986insACA , CM000671.2:g.114402985_114402986insACA	GRCh38
NC_000009.11:g.117165265_117165266insACA , CM000671.1:g.117165265_117165266insACA	GRCh37
NC_000009.10:g.116205086_116205087insACA	NCBI36
NG_016700.1:g.107471_107472insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.886-50_886-49insTGT	ENSP00000514396.1:n.886-50_886-49insTGT
ENST00000362057.4:c.2542-50_2542-49insTGT MANE Select	ENSP00000354623.3:n.2542-50_2542-49insTGT
ENST00000674036.8:c.1515-50_1515-49insTGT
ENST00000674048.1:n.2423-50_2423-49insTGT
ENST00000265134.10:c.1393-50_1393-49insTGT	ENSP00000265134.6:n.1393-50_1393-49insTGT
ENST00000362057.3:c.2542-50_2542-49insTGT	ENSP00000354623.3:n.2542-50_2542-49insTGT
ENST00000374059.7:c.1489-50_1489-49insTGT	ENSP00000363172.3:n.1489-50_1489-49insTGT
NM_001083885.2:c.1393-50_1393-49insTGT	NP_001077354.2:n.1393-50_1393-49insTGT
NM_001173425.1:c.2539-50_2539-49insTGT	NP_001166896.1:n.2539-50_2539-49insTGT
NM_015404.3:c.2542-50_2542-49insTGT	NP_056219.3:n.2542-50_2542-49insTGT
XM_005251897.3:c.1879-50_1879-49insTGT	XP_005251954.2:n.1879-50_1879-49insTGT
XM_011518484.1:c.2575-50_2575-49insTGT	XP_011516786.1:n.2575-50_2575-49insTGT
XM_011518485.1:c.2575-50_2575-49insTGT	XP_011516787.1:n.2575-50_2575-49insTGT
XM_011518486.1:c.2572-50_2572-49insTGT	XP_011516788.1:n.2572-50_2572-49insTGT
XM_011518487.1:c.2449-50_2449-49insTGT	XP_011516789.1:n.2449-50_2449-49insTGT
XM_011518488.1:c.2332-50_2332-49insTGT	XP_011516790.1:n.2332-50_2332-49insTGT
XM_011518495.1:c.1252-50_1252-49insTGT	XP_011516797.1:n.1252-50_1252-49insTGT
XR_929747.1:n.3479-50_3479-49insTGT
XR_929748.1:n.3377-50_3377-49insTGT
NM_001346890.1:c.1489-50_1489-49insTGT	NP_001333819.1:n.1489-50_1489-49insTGT
XM_011518486.2:c.2572-50_2572-49insTGT	XP_011516788.1:n.2572-50_2572-49insTGT
XM_011518487.2:c.2449-50_2449-49insTGT	XP_011516789.1:n.2449-50_2449-49insTGT
XM_011518488.2:c.2332-50_2332-49insTGT	XP_011516790.1:n.2332-50_2332-49insTGT
XR_929747.2:n.2790-50_2790-49insTGT
XR_929748.2:n.2688-50_2688-49insTGT
NM_015404.4:c.2542-50_2542-49insTGT MANE Select	NP_056219.3:n.2542-50_2542-49insTGT
NM_001173425.2:c.2539-50_2539-49insTGT	NP_001166896.1:n.2539-50_2539-49insTGT
NM_001083885.3:c.1393-50_1393-49insTGT	NP_001077354.2:n.1393-50_1393-49insTGT