Canonical Allele Identifier: CA1873826054

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404297_114404298delinsAG , CM000671.2:g.114404297_114404298delinsAG	GRCh38
NC_000009.11:g.117166577_117166578delinsAG , CM000671.1:g.117166577_117166578delinsAG	GRCh37
NC_000009.10:g.116206398_116206399delinsAG	NCBI36
NG_016700.1:g.106159_106160delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.581-221_581-220delinsCT	ENSP00000514396.1:n.581-221_581-220delinsCT
ENST00000362057.4:c.2237-221_2237-220delinsCT MANE Select	ENSP00000354623.3:n.2237-221_2237-220delinsCT
ENST00000674036.8:c.1210-221_1210-220delinsCT
ENST00000674048.1:n.2118-221_2118-220delinsCT
ENST00000265134.10:c.1088-221_1088-220delinsCT	ENSP00000265134.6:n.1088-221_1088-220delinsCT
ENST00000362057.3:c.2237-221_2237-220delinsCT	ENSP00000354623.3:n.2237-221_2237-220delinsCT
ENST00000374059.7:c.1184-221_1184-220delinsCT	ENSP00000363172.3:n.1184-221_1184-220delinsCT
NM_001083885.2:c.1088-221_1088-220delinsCT	NP_001077354.2:n.1088-221_1088-220delinsCT
NM_001173425.1:c.2237-224_2237-223delinsCT	NP_001166896.1:n.2237-224_2237-223delinsCT
NM_015404.3:c.2237-221_2237-220delinsCT	NP_056219.3:n.2237-221_2237-220delinsCT
XM_005251897.3:c.1574-221_1574-220delinsCT	XP_005251954.2:n.1574-221_1574-220delinsCT
XM_011518484.1:c.2270-221_2270-220delinsCT	XP_011516786.1:n.2270-221_2270-220delinsCT
XM_011518485.1:c.2270-221_2270-220delinsCT	XP_011516787.1:n.2270-221_2270-220delinsCT
XM_011518486.1:c.2270-224_2270-223delinsCT	XP_011516788.1:n.2270-224_2270-223delinsCT
XM_011518487.1:c.2144-221_2144-220delinsCT	XP_011516789.1:n.2144-221_2144-220delinsCT
XM_011518488.1:c.2027-221_2027-220delinsCT	XP_011516790.1:n.2027-221_2027-220delinsCT
XM_011518495.1:c.947-221_947-220delinsCT	XP_011516797.1:n.947-221_947-220delinsCT
XR_929747.1:n.3174-221_3174-220delinsCT
XR_929748.1:n.3072-221_3072-220delinsCT
NM_001346890.1:c.1184-221_1184-220delinsCT	NP_001333819.1:n.1184-221_1184-220delinsCT
XM_011518486.2:c.2270-224_2270-223delinsCT	XP_011516788.1:n.2270-224_2270-223delinsCT
XM_011518487.2:c.2144-221_2144-220delinsCT	XP_011516789.1:n.2144-221_2144-220delinsCT
XM_011518488.2:c.2027-221_2027-220delinsCT	XP_011516790.1:n.2027-221_2027-220delinsCT
XR_929747.2:n.2485-221_2485-220delinsCT
XR_929748.2:n.2383-221_2383-220delinsCT
NM_015404.4:c.2237-221_2237-220delinsCT MANE Select	NP_056219.3:n.2237-221_2237-220delinsCT
NM_001173425.2:c.2237-224_2237-223delinsCT	NP_001166896.1:n.2237-224_2237-223delinsCT
NM_001083885.3:c.1088-221_1088-220delinsCT	NP_001077354.2:n.1088-221_1088-220delinsCT