Canonical Allele Identifier: CA1873834995
Gene: WHRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114424024_114424026delinsCCA , CM000671.2:g.114424024_114424026delinsCCA GRCh38
NC_000009.11:g.117186304_117186306delinsCCA , CM000671.1:g.117186304_117186306delinsCCA GRCh37
NC_000009.10:g.116226125_116226127delinsCCA NCBI36
NG_016700.1:g.86431_86433delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000699486.1:c.1140+308_1140+310delinsTGG ENSP00000514397.1:n.1140+308_1140+310delinsTGG
ENST00000362057.4:c.1416+308_1416+310delinsTGG MANE Select ENSP00000354623.3:n.1416+308_1416+310delinsTGG
ENST00000673811.1:n.2350+308_2350+310delinsTGG
ENST00000674036.8:c.599+308_599+310delinsTGG
ENST00000674048.1:n.1297+308_1297+310delinsTGG
ENST00000265134.10:c.267+308_267+310delinsTGG ENSP00000265134.6:n.267+308_267+310delinsTGG
ENST00000362057.3:c.1416+308_1416+310delinsTGG ENSP00000354623.3:n.1416+308_1416+310delinsTGG
ENST00000374059.7:c.363+308_363+310delinsTGG ENSP00000363172.3:n.363+308_363+310delinsTGG
NM_001083885.2:c.267+308_267+310delinsTGG NP_001077354.2:n.267+308_267+310delinsTGG
NM_001173425.1:c.1416+308_1416+310delinsTGG NP_001166896.1:n.1416+308_1416+310delinsTGG
NM_015404.3:c.1416+308_1416+310delinsTGG NP_056219.3:n.1416+308_1416+310delinsTGG
XM_005251897.3:c.964-16008_964-16006delinsTGG XP_005251954.2:n.964-16008_964-16006delinsTGG
XM_011518484.1:c.1416+308_1416+310delinsTGG XP_011516786.1:n.1416+308_1416+310delinsTGG
XM_011518485.1:c.1416+308_1416+310delinsTGG XP_011516787.1:n.1416+308_1416+310delinsTGG
XM_011518486.1:c.1416+308_1416+310delinsTGG XP_011516788.1:n.1416+308_1416+310delinsTGG
XM_011518487.1:c.1290+308_1290+310delinsTGG XP_011516789.1:n.1290+308_1290+310delinsTGG
XM_011518488.1:c.1416+308_1416+310delinsTGG XP_011516790.1:n.1416+308_1416+310delinsTGG
XM_011518489.1:c.1416+308_1416+310delinsTGG XP_011516791.1:n.1416+308_1416+310delinsTGG
XM_011518490.1:c.1416+308_1416+310delinsTGG XP_011516792.1:n.1416+308_1416+310delinsTGG
XM_011518491.1:c.1416+308_1416+310delinsTGG XP_011516793.1:n.1416+308_1416+310delinsTGG
XM_011518492.1:c.1416+308_1416+310delinsTGG XP_011516794.1:n.1416+308_1416+310delinsTGG
XM_011518493.1:c.1416+308_1416+310delinsTGG XP_011516795.1:n.1416+308_1416+310delinsTGG
XM_011518494.1:c.1416+308_1416+310delinsTGG XP_011516796.1:n.1416+308_1416+310delinsTGG
XM_011518495.1:c.93+308_93+310delinsTGG XP_011516797.1:n.93+308_93+310delinsTGG
XR_929747.1:n.2124+308_2124+310delinsTGG
XR_929748.1:n.2124+308_2124+310delinsTGG
XR_929749.1:n.2124+308_2124+310delinsTGG
XR_929750.1:n.2124+308_2124+310delinsTGG
XR_929751.1:n.2124+308_2124+310delinsTGG
XR_929752.1:n.2124+308_2124+310delinsTGG
XR_929753.1:n.2124+308_2124+310delinsTGG
XR_929754.1:n.2124+308_2124+310delinsTGG
XR_929755.1:n.2124+308_2124+310delinsTGG
XR_929756.1:n.2124+308_2124+310delinsTGG
XR_929757.1:n.2124+308_2124+310delinsTGG
NM_001346890.1:c.363+308_363+310delinsTGG NP_001333819.1:n.363+308_363+310delinsTGG
XM_011518486.2:c.1416+308_1416+310delinsTGG XP_011516788.1:n.1416+308_1416+310delinsTGG
XM_011518487.2:c.1290+308_1290+310delinsTGG XP_011516789.1:n.1290+308_1290+310delinsTGG
XM_011518488.2:c.1416+308_1416+310delinsTGG XP_011516790.1:n.1416+308_1416+310delinsTGG
XM_011518489.3:c.1416+308_1416+310delinsTGG XP_011516791.1:n.1416+308_1416+310delinsTGG
XM_011518491.3:c.1416+308_1416+310delinsTGG XP_011516793.1:n.1416+308_1416+310delinsTGG
XM_011518492.2:c.1416+308_1416+310delinsTGG XP_011516794.1:n.1416+308_1416+310delinsTGG
XM_011518494.3:c.1416+308_1416+310delinsTGG XP_011516796.1:n.1416+308_1416+310delinsTGG
XR_929747.2:n.1435+308_1435+310delinsTGG
XR_929748.2:n.1435+308_1435+310delinsTGG
XR_929749.2:n.1435+308_1435+310delinsTGG
XR_929750.3:n.1435+308_1435+310delinsTGG
XR_929752.2:n.1435+308_1435+310delinsTGG
XR_929753.3:n.1435+308_1435+310delinsTGG
XR_929754.2:n.1435+308_1435+310delinsTGG
XR_929755.3:n.1435+308_1435+310delinsTGG
XR_929756.2:n.1435+308_1435+310delinsTGG
XR_929757.2:n.1435+308_1435+310delinsTGG
NM_015404.4:c.1416+308_1416+310delinsTGG MANE Select NP_056219.3:n.1416+308_1416+310delinsTGG
NM_001173425.2:c.1416+308_1416+310delinsTGG NP_001166896.1:n.1416+308_1416+310delinsTGG
NM_001083885.3:c.267+308_267+310delinsTGG NP_001077354.2:n.267+308_267+310delinsTGG