Canonical Allele Identifier: CA1873825456

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403090_114403092delinsGGT , CM000671.2:g.114403090_114403092delinsGGT	GRCh38
NC_000009.11:g.117165370_117165372delinsGGT , CM000671.1:g.117165370_117165372delinsGGT	GRCh37
NC_000009.10:g.116205191_116205193delinsGGT	NCBI36
NG_016700.1:g.107365_107367delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.885+125_885+127delinsACC	ENSP00000514396.1:n.885+125_885+127delinsACC
ENST00000362057.4:c.2541+125_2541+127delinsACC MANE Select	ENSP00000354623.3:n.2541+125_2541+127delinsACC
ENST00000674036.8:c.1514+125_1514+127delinsACC
ENST00000674048.1:n.2422+125_2422+127delinsACC
ENST00000265134.10:c.1392+125_1392+127delinsACC	ENSP00000265134.6:n.1392+125_1392+127delinsACC
ENST00000362057.3:c.2541+125_2541+127delinsACC	ENSP00000354623.3:n.2541+125_2541+127delinsACC
ENST00000374059.7:c.1488+125_1488+127delinsACC	ENSP00000363172.3:n.1488+125_1488+127delinsACC
NM_001083885.2:c.1392+125_1392+127delinsACC	NP_001077354.2:n.1392+125_1392+127delinsACC
NM_001173425.1:c.2538+125_2538+127delinsACC	NP_001166896.1:n.2538+125_2538+127delinsACC
NM_015404.3:c.2541+125_2541+127delinsACC	NP_056219.3:n.2541+125_2541+127delinsACC
XM_005251897.3:c.1878+125_1878+127delinsACC	XP_005251954.2:n.1878+125_1878+127delinsACC
XM_011518484.1:c.2574+125_2574+127delinsACC	XP_011516786.1:n.2574+125_2574+127delinsACC
XM_011518485.1:c.2574+125_2574+127delinsACC	XP_011516787.1:n.2574+125_2574+127delinsACC
XM_011518486.1:c.2571+125_2571+127delinsACC	XP_011516788.1:n.2571+125_2571+127delinsACC
XM_011518487.1:c.2448+125_2448+127delinsACC	XP_011516789.1:n.2448+125_2448+127delinsACC
XM_011518488.1:c.2331+125_2331+127delinsACC	XP_011516790.1:n.2331+125_2331+127delinsACC
XM_011518495.1:c.1251+125_1251+127delinsACC	XP_011516797.1:n.1251+125_1251+127delinsACC
XR_929747.1:n.3478+125_3478+127delinsACC
XR_929748.1:n.3376+125_3376+127delinsACC
NM_001346890.1:c.1488+125_1488+127delinsACC	NP_001333819.1:n.1488+125_1488+127delinsACC
XM_011518486.2:c.2571+125_2571+127delinsACC	XP_011516788.1:n.2571+125_2571+127delinsACC
XM_011518487.2:c.2448+125_2448+127delinsACC	XP_011516789.1:n.2448+125_2448+127delinsACC
XM_011518488.2:c.2331+125_2331+127delinsACC	XP_011516790.1:n.2331+125_2331+127delinsACC
XR_929747.2:n.2789+125_2789+127delinsACC
XR_929748.2:n.2687+125_2687+127delinsACC
NM_015404.4:c.2541+125_2541+127delinsACC MANE Select	NP_056219.3:n.2541+125_2541+127delinsACC
NM_001173425.2:c.2538+125_2538+127delinsACC	NP_001166896.1:n.2538+125_2538+127delinsACC
NM_001083885.3:c.1392+125_1392+127delinsACC	NP_001077354.2:n.1392+125_1392+127delinsACC