Canonical Allele Identifier: CA1873835906

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114425925_114425929delinsCCCCA , CM000671.2:g.114425925_114425929delinsCCCCA	GRCh38
NC_000009.11:g.117188205_117188209delinsCCCCA , CM000671.1:g.117188205_117188209delinsCCCCA	GRCh37
NC_000009.10:g.116228026_116228030delinsCCCCA	NCBI36
NG_016700.1:g.84528_84532delinsTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.890+282_890+286delinsTGGGG	ENSP00000514397.1:n.890+282_890+286delinsTGGGG
ENST00000362057.4:c.1166+282_1166+286delinsTGGGG MANE Select	ENSP00000354623.3:n.1166+282_1166+286delinsTGGGG
ENST00000673811.1:n.1196_1200delinsTGGGG
ENST00000674036.8:c.349+282_349+286delinsTGGGG
ENST00000674048.1:n.143_147delinsTGGGG
ENST00000265134.10:c.17+282_17+286delinsTGGGG	ENSP00000265134.6:n.17+282_17+286delinsTGGGG
ENST00000362057.3:c.1166+282_1166+286delinsTGGGG	ENSP00000354623.3:n.1166+282_1166+286delinsTGGGG
ENST00000374059.7:c.-792_-788delinsTGGGG	ENSP00000363172.3:n.-792_-788delinsTGGGG
NM_001083885.2:c.17+282_17+286delinsTGGGG	NP_001077354.2:n.17+282_17+286delinsTGGGG
NM_001173425.1:c.1166+282_1166+286delinsTGGGG	NP_001166896.1:n.1166+282_1166+286delinsTGGGG
NM_015404.3:c.1166+282_1166+286delinsTGGGG	NP_056219.3:n.1166+282_1166+286delinsTGGGG
XM_005251897.3:c.964-17911_964-17907delinsTGGGG	XP_005251954.2:n.964-17911_964-17907delinsTGGGG
XM_011518484.1:c.1166+282_1166+286delinsTGGGG	XP_011516786.1:n.1166+282_1166+286delinsTGGGG
XM_011518485.1:c.1166+282_1166+286delinsTGGGG	XP_011516787.1:n.1166+282_1166+286delinsTGGGG
XM_011518486.1:c.1166+282_1166+286delinsTGGGG	XP_011516788.1:n.1166+282_1166+286delinsTGGGG
XM_011518487.1:c.1040+282_1040+286delinsTGGGG	XP_011516789.1:n.1040+282_1040+286delinsTGGGG
XM_011518488.1:c.1166+282_1166+286delinsTGGGG	XP_011516790.1:n.1166+282_1166+286delinsTGGGG
XM_011518489.1:c.1166+282_1166+286delinsTGGGG	XP_011516791.1:n.1166+282_1166+286delinsTGGGG
XM_011518490.1:c.1166+282_1166+286delinsTGGGG	XP_011516792.1:n.1166+282_1166+286delinsTGGGG
XM_011518491.1:c.1166+282_1166+286delinsTGGGG	XP_011516793.1:n.1166+282_1166+286delinsTGGGG
XM_011518492.1:c.1166+282_1166+286delinsTGGGG	XP_011516794.1:n.1166+282_1166+286delinsTGGGG
XM_011518493.1:c.1166+282_1166+286delinsTGGGG	XP_011516795.1:n.1166+282_1166+286delinsTGGGG
XM_011518494.1:c.1166+282_1166+286delinsTGGGG	XP_011516796.1:n.1166+282_1166+286delinsTGGGG
XM_011518495.1:c.-157-905_-157-901delinsTGGGG	XP_011516797.1:n.-157-905_-157-901delinsTGGGG
XR_929747.1:n.1874+282_1874+286delinsTGGGG
XR_929748.1:n.1874+282_1874+286delinsTGGGG
XR_929749.1:n.1874+282_1874+286delinsTGGGG
XR_929750.1:n.1874+282_1874+286delinsTGGGG
XR_929751.1:n.1874+282_1874+286delinsTGGGG
XR_929752.1:n.1874+282_1874+286delinsTGGGG
XR_929753.1:n.1874+282_1874+286delinsTGGGG
XR_929754.1:n.1874+282_1874+286delinsTGGGG
XR_929755.1:n.1874+282_1874+286delinsTGGGG
XR_929756.1:n.1874+282_1874+286delinsTGGGG
XR_929757.1:n.1874+282_1874+286delinsTGGGG
NM_001346890.1:c.-792_-788delinsTGGGG	NP_001333819.1:n.-792_-788delinsTGGGG
XM_011518486.2:c.1166+282_1166+286delinsTGGGG	XP_011516788.1:n.1166+282_1166+286delinsTGGGG
XM_011518487.2:c.1040+282_1040+286delinsTGGGG	XP_011516789.1:n.1040+282_1040+286delinsTGGGG
XM_011518488.2:c.1166+282_1166+286delinsTGGGG	XP_011516790.1:n.1166+282_1166+286delinsTGGGG
XM_011518489.3:c.1166+282_1166+286delinsTGGGG	XP_011516791.1:n.1166+282_1166+286delinsTGGGG
XM_011518491.3:c.1166+282_1166+286delinsTGGGG	XP_011516793.1:n.1166+282_1166+286delinsTGGGG
XM_011518492.2:c.1166+282_1166+286delinsTGGGG	XP_011516794.1:n.1166+282_1166+286delinsTGGGG
XM_011518494.3:c.1166+282_1166+286delinsTGGGG	XP_011516796.1:n.1166+282_1166+286delinsTGGGG
XR_929747.2:n.1185+282_1185+286delinsTGGGG
XR_929748.2:n.1185+282_1185+286delinsTGGGG
XR_929749.2:n.1185+282_1185+286delinsTGGGG
XR_929750.3:n.1185+282_1185+286delinsTGGGG
XR_929752.2:n.1185+282_1185+286delinsTGGGG
XR_929753.3:n.1185+282_1185+286delinsTGGGG
XR_929754.2:n.1185+282_1185+286delinsTGGGG
XR_929755.3:n.1185+282_1185+286delinsTGGGG
XR_929756.2:n.1185+282_1185+286delinsTGGGG
XR_929757.2:n.1185+282_1185+286delinsTGGGG
NM_015404.4:c.1166+282_1166+286delinsTGGGG MANE Select	NP_056219.3:n.1166+282_1166+286delinsTGGGG
NM_001173425.2:c.1166+282_1166+286delinsTGGGG	NP_001166896.1:n.1166+282_1166+286delinsTGGGG
NM_001083885.3:c.17+282_17+286delinsTGGGG	NP_001077354.2:n.17+282_17+286delinsTGGGG