Canonical Allele Identifier: CA2691374250

Gene: WHRN

Linked Data

• gnomAD v4: 9-114425874-CCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114425877_114425879del , CM000671.2:g.114425877_114425879del	GRCh38
NC_000009.11:g.117188157_117188159del , CM000671.1:g.117188157_117188159del	GRCh37
NC_000009.10:g.116227978_116227980del	NCBI36
NG_016700.1:g.84580_84582del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.890+334_890+336del	ENSP00000514397.1:n.890+334_890+336del
ENST00000362057.4:c.1166+334_1166+336del MANE Select	ENSP00000354623.3:n.1166+334_1166+336del
ENST00000673811.1:n.1248_1250del
ENST00000674036.8:c.349+334_349+336del
ENST00000674048.1:n.195_197del
ENST00000265134.10:c.17+334_17+336del	ENSP00000265134.6:n.17+334_17+336del
ENST00000362057.3:c.1166+334_1166+336del	ENSP00000354623.3:n.1166+334_1166+336del
ENST00000374059.7:c.-740_-738del	ENSP00000363172.3:n.-740_-738del
NM_001083885.2:c.17+334_17+336del	NP_001077354.2:n.17+334_17+336del
NM_001173425.1:c.1166+334_1166+336del	NP_001166896.1:n.1166+334_1166+336del
NM_015404.3:c.1166+334_1166+336del	NP_056219.3:n.1166+334_1166+336del
XM_005251897.3:c.964-17859_964-17857del	XP_005251954.2:n.964-17859_964-17857del
XM_011518484.1:c.1166+334_1166+336del	XP_011516786.1:n.1166+334_1166+336del
XM_011518485.1:c.1166+334_1166+336del	XP_011516787.1:n.1166+334_1166+336del
XM_011518486.1:c.1166+334_1166+336del	XP_011516788.1:n.1166+334_1166+336del
XM_011518487.1:c.1040+334_1040+336del	XP_011516789.1:n.1040+334_1040+336del
XM_011518488.1:c.1166+334_1166+336del	XP_011516790.1:n.1166+334_1166+336del
XM_011518489.1:c.1166+334_1166+336del	XP_011516791.1:n.1166+334_1166+336del
XM_011518490.1:c.1166+334_1166+336del	XP_011516792.1:n.1166+334_1166+336del
XM_011518491.1:c.1166+334_1166+336del	XP_011516793.1:n.1166+334_1166+336del
XM_011518492.1:c.1166+334_1166+336del	XP_011516794.1:n.1166+334_1166+336del
XM_011518493.1:c.1166+334_1166+336del	XP_011516795.1:n.1166+334_1166+336del
XM_011518494.1:c.1166+334_1166+336del	XP_011516796.1:n.1166+334_1166+336del
XM_011518495.1:c.-157-853_-157-851del	XP_011516797.1:n.-157-853_-157-851del
XR_929747.1:n.1874+334_1874+336del
XR_929748.1:n.1874+334_1874+336del
XR_929749.1:n.1874+334_1874+336del
XR_929750.1:n.1874+334_1874+336del
XR_929751.1:n.1874+334_1874+336del
XR_929752.1:n.1874+334_1874+336del
XR_929753.1:n.1874+334_1874+336del
XR_929754.1:n.1874+334_1874+336del
XR_929755.1:n.1874+334_1874+336del
XR_929756.1:n.1874+334_1874+336del
XR_929757.1:n.1874+334_1874+336del
NM_001346890.1:c.-740_-738del	NP_001333819.1:n.-740_-738del
XM_011518486.2:c.1166+334_1166+336del	XP_011516788.1:n.1166+334_1166+336del
XM_011518487.2:c.1040+334_1040+336del	XP_011516789.1:n.1040+334_1040+336del
XM_011518488.2:c.1166+334_1166+336del	XP_011516790.1:n.1166+334_1166+336del
XM_011518489.3:c.1166+334_1166+336del	XP_011516791.1:n.1166+334_1166+336del
XM_011518491.3:c.1166+334_1166+336del	XP_011516793.1:n.1166+334_1166+336del
XM_011518492.2:c.1166+334_1166+336del	XP_011516794.1:n.1166+334_1166+336del
XM_011518494.3:c.1166+334_1166+336del	XP_011516796.1:n.1166+334_1166+336del
XR_929747.2:n.1185+334_1185+336del
XR_929748.2:n.1185+334_1185+336del
XR_929749.2:n.1185+334_1185+336del
XR_929750.3:n.1185+334_1185+336del
XR_929752.2:n.1185+334_1185+336del
XR_929753.3:n.1185+334_1185+336del
XR_929754.2:n.1185+334_1185+336del
XR_929755.3:n.1185+334_1185+336del
XR_929756.2:n.1185+334_1185+336del
XR_929757.2:n.1185+334_1185+336del
NM_015404.4:c.1166+334_1166+336del MANE Select	NP_056219.3:n.1166+334_1166+336del
NM_001173425.2:c.1166+334_1166+336del	NP_001166896.1:n.1166+334_1166+336del
NM_001083885.3:c.17+334_17+336del	NP_001077354.2:n.17+334_17+336del