Canonical Allele Identifier: CA1873825963

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404107_114404109delinsGCT , CM000671.2:g.114404107_114404109delinsGCT	GRCh38
NC_000009.11:g.117166387_117166389delinsGCT , CM000671.1:g.117166387_117166389delinsGCT	GRCh37
NC_000009.10:g.116206208_116206210delinsGCT	NCBI36
NG_016700.1:g.106348_106350delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.581-32_581-30delinsAGC	ENSP00000514396.1:n.581-32_581-30delinsAGC
ENST00000362057.4:c.2237-32_2237-30delinsAGC MANE Select	ENSP00000354623.3:n.2237-32_2237-30delinsAGC
ENST00000674036.8:c.1210-32_1210-30delinsAGC
ENST00000674048.1:n.2118-32_2118-30delinsAGC
ENST00000265134.10:c.1088-32_1088-30delinsAGC	ENSP00000265134.6:n.1088-32_1088-30delinsAGC
ENST00000362057.3:c.2237-32_2237-30delinsAGC	ENSP00000354623.3:n.2237-32_2237-30delinsAGC
ENST00000374059.7:c.1184-32_1184-30delinsAGC	ENSP00000363172.3:n.1184-32_1184-30delinsAGC
NM_001083885.2:c.1088-32_1088-30delinsAGC	NP_001077354.2:n.1088-32_1088-30delinsAGC
NM_001173425.1:c.2237-35_2237-33delinsAGC	NP_001166896.1:n.2237-35_2237-33delinsAGC
NM_015404.3:c.2237-32_2237-30delinsAGC	NP_056219.3:n.2237-32_2237-30delinsAGC
XM_005251897.3:c.1574-32_1574-30delinsAGC	XP_005251954.2:n.1574-32_1574-30delinsAGC
XM_011518484.1:c.2270-32_2270-30delinsAGC	XP_011516786.1:n.2270-32_2270-30delinsAGC
XM_011518485.1:c.2270-32_2270-30delinsAGC	XP_011516787.1:n.2270-32_2270-30delinsAGC
XM_011518486.1:c.2270-35_2270-33delinsAGC	XP_011516788.1:n.2270-35_2270-33delinsAGC
XM_011518487.1:c.2144-32_2144-30delinsAGC	XP_011516789.1:n.2144-32_2144-30delinsAGC
XM_011518488.1:c.2027-32_2027-30delinsAGC	XP_011516790.1:n.2027-32_2027-30delinsAGC
XM_011518495.1:c.947-32_947-30delinsAGC	XP_011516797.1:n.947-32_947-30delinsAGC
XR_929747.1:n.3174-32_3174-30delinsAGC
XR_929748.1:n.3072-32_3072-30delinsAGC
NM_001346890.1:c.1184-32_1184-30delinsAGC	NP_001333819.1:n.1184-32_1184-30delinsAGC
XM_011518486.2:c.2270-35_2270-33delinsAGC	XP_011516788.1:n.2270-35_2270-33delinsAGC
XM_011518487.2:c.2144-32_2144-30delinsAGC	XP_011516789.1:n.2144-32_2144-30delinsAGC
XM_011518488.2:c.2027-32_2027-30delinsAGC	XP_011516790.1:n.2027-32_2027-30delinsAGC
XR_929747.2:n.2485-32_2485-30delinsAGC
XR_929748.2:n.2383-32_2383-30delinsAGC
NM_015404.4:c.2237-32_2237-30delinsAGC MANE Select	NP_056219.3:n.2237-32_2237-30delinsAGC
NM_001173425.2:c.2237-35_2237-33delinsAGC	NP_001166896.1:n.2237-35_2237-33delinsAGC
NM_001083885.3:c.1088-32_1088-30delinsAGC	NP_001077354.2:n.1088-32_1088-30delinsAGC