Canonical Allele Identifier: CA1873826007

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404185_114404186delinsAG , CM000671.2:g.114404185_114404186delinsAG	GRCh38
NC_000009.11:g.117166465_117166466delinsAG , CM000671.1:g.117166465_117166466delinsAG	GRCh37
NC_000009.10:g.116206286_116206287delinsAG	NCBI36
NG_016700.1:g.106271_106272delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.581-109_581-108delinsCT	ENSP00000514396.1:n.581-109_581-108delinsCT
ENST00000362057.4:c.2237-109_2237-108delinsCT MANE Select	ENSP00000354623.3:n.2237-109_2237-108delinsCT
ENST00000674036.8:c.1210-109_1210-108delinsCT
ENST00000674048.1:n.2118-109_2118-108delinsCT
ENST00000265134.10:c.1088-109_1088-108delinsCT	ENSP00000265134.6:n.1088-109_1088-108delinsCT
ENST00000362057.3:c.2237-109_2237-108delinsCT	ENSP00000354623.3:n.2237-109_2237-108delinsCT
ENST00000374059.7:c.1184-109_1184-108delinsCT	ENSP00000363172.3:n.1184-109_1184-108delinsCT
NM_001083885.2:c.1088-109_1088-108delinsCT	NP_001077354.2:n.1088-109_1088-108delinsCT
NM_001173425.1:c.2237-112_2237-111delinsCT	NP_001166896.1:n.2237-112_2237-111delinsCT
NM_015404.3:c.2237-109_2237-108delinsCT	NP_056219.3:n.2237-109_2237-108delinsCT
XM_005251897.3:c.1574-109_1574-108delinsCT	XP_005251954.2:n.1574-109_1574-108delinsCT
XM_011518484.1:c.2270-109_2270-108delinsCT	XP_011516786.1:n.2270-109_2270-108delinsCT
XM_011518485.1:c.2270-109_2270-108delinsCT	XP_011516787.1:n.2270-109_2270-108delinsCT
XM_011518486.1:c.2270-112_2270-111delinsCT	XP_011516788.1:n.2270-112_2270-111delinsCT
XM_011518487.1:c.2144-109_2144-108delinsCT	XP_011516789.1:n.2144-109_2144-108delinsCT
XM_011518488.1:c.2027-109_2027-108delinsCT	XP_011516790.1:n.2027-109_2027-108delinsCT
XM_011518495.1:c.947-109_947-108delinsCT	XP_011516797.1:n.947-109_947-108delinsCT
XR_929747.1:n.3174-109_3174-108delinsCT
XR_929748.1:n.3072-109_3072-108delinsCT
NM_001346890.1:c.1184-109_1184-108delinsCT	NP_001333819.1:n.1184-109_1184-108delinsCT
XM_011518486.2:c.2270-112_2270-111delinsCT	XP_011516788.1:n.2270-112_2270-111delinsCT
XM_011518487.2:c.2144-109_2144-108delinsCT	XP_011516789.1:n.2144-109_2144-108delinsCT
XM_011518488.2:c.2027-109_2027-108delinsCT	XP_011516790.1:n.2027-109_2027-108delinsCT
XR_929747.2:n.2485-109_2485-108delinsCT
XR_929748.2:n.2383-109_2383-108delinsCT
NM_015404.4:c.2237-109_2237-108delinsCT MANE Select	NP_056219.3:n.2237-109_2237-108delinsCT
NM_001173425.2:c.2237-112_2237-111delinsCT	NP_001166896.1:n.2237-112_2237-111delinsCT
NM_001083885.3:c.1088-109_1088-108delinsCT	NP_001077354.2:n.1088-109_1088-108delinsCT