Canonical Allele Identifier: CA2691374257

Gene: WHRN

Linked Data

• gnomAD v4: 9-114425879-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114425884_114425885del , CM000671.2:g.114425884_114425885del	GRCh38
NC_000009.11:g.117188164_117188165del , CM000671.1:g.117188164_117188165del	GRCh37
NC_000009.10:g.116227985_116227986del	NCBI36
NG_016700.1:g.84576_84577del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.890+330_890+331del	ENSP00000514397.1:n.890+330_890+331del
ENST00000362057.4:c.1166+330_1166+331del MANE Select	ENSP00000354623.3:n.1166+330_1166+331del
ENST00000673811.1:n.1244_1245del
ENST00000674036.8:c.349+330_349+331del
ENST00000674048.1:n.191_192del
ENST00000265134.10:c.17+330_17+331del	ENSP00000265134.6:n.17+330_17+331del
ENST00000362057.3:c.1166+330_1166+331del	ENSP00000354623.3:n.1166+330_1166+331del
ENST00000374059.7:c.-744_-743del	ENSP00000363172.3:n.-744_-743del
NM_001083885.2:c.17+330_17+331del	NP_001077354.2:n.17+330_17+331del
NM_001173425.1:c.1166+330_1166+331del	NP_001166896.1:n.1166+330_1166+331del
NM_015404.3:c.1166+330_1166+331del	NP_056219.3:n.1166+330_1166+331del
XM_005251897.3:c.964-17863_964-17862del	XP_005251954.2:n.964-17863_964-17862del
XM_011518484.1:c.1166+330_1166+331del	XP_011516786.1:n.1166+330_1166+331del
XM_011518485.1:c.1166+330_1166+331del	XP_011516787.1:n.1166+330_1166+331del
XM_011518486.1:c.1166+330_1166+331del	XP_011516788.1:n.1166+330_1166+331del
XM_011518487.1:c.1040+330_1040+331del	XP_011516789.1:n.1040+330_1040+331del
XM_011518488.1:c.1166+330_1166+331del	XP_011516790.1:n.1166+330_1166+331del
XM_011518489.1:c.1166+330_1166+331del	XP_011516791.1:n.1166+330_1166+331del
XM_011518490.1:c.1166+330_1166+331del	XP_011516792.1:n.1166+330_1166+331del
XM_011518491.1:c.1166+330_1166+331del	XP_011516793.1:n.1166+330_1166+331del
XM_011518492.1:c.1166+330_1166+331del	XP_011516794.1:n.1166+330_1166+331del
XM_011518493.1:c.1166+330_1166+331del	XP_011516795.1:n.1166+330_1166+331del
XM_011518494.1:c.1166+330_1166+331del	XP_011516796.1:n.1166+330_1166+331del
XM_011518495.1:c.-157-857_-157-856del	XP_011516797.1:n.-157-857_-157-856del
XR_929747.1:n.1874+330_1874+331del
XR_929748.1:n.1874+330_1874+331del
XR_929749.1:n.1874+330_1874+331del
XR_929750.1:n.1874+330_1874+331del
XR_929751.1:n.1874+330_1874+331del
XR_929752.1:n.1874+330_1874+331del
XR_929753.1:n.1874+330_1874+331del
XR_929754.1:n.1874+330_1874+331del
XR_929755.1:n.1874+330_1874+331del
XR_929756.1:n.1874+330_1874+331del
XR_929757.1:n.1874+330_1874+331del
NM_001346890.1:c.-744_-743del	NP_001333819.1:n.-744_-743del
XM_011518486.2:c.1166+330_1166+331del	XP_011516788.1:n.1166+330_1166+331del
XM_011518487.2:c.1040+330_1040+331del	XP_011516789.1:n.1040+330_1040+331del
XM_011518488.2:c.1166+330_1166+331del	XP_011516790.1:n.1166+330_1166+331del
XM_011518489.3:c.1166+330_1166+331del	XP_011516791.1:n.1166+330_1166+331del
XM_011518491.3:c.1166+330_1166+331del	XP_011516793.1:n.1166+330_1166+331del
XM_011518492.2:c.1166+330_1166+331del	XP_011516794.1:n.1166+330_1166+331del
XM_011518494.3:c.1166+330_1166+331del	XP_011516796.1:n.1166+330_1166+331del
XR_929747.2:n.1185+330_1185+331del
XR_929748.2:n.1185+330_1185+331del
XR_929749.2:n.1185+330_1185+331del
XR_929750.3:n.1185+330_1185+331del
XR_929752.2:n.1185+330_1185+331del
XR_929753.3:n.1185+330_1185+331del
XR_929754.2:n.1185+330_1185+331del
XR_929755.3:n.1185+330_1185+331del
XR_929756.2:n.1185+330_1185+331del
XR_929757.2:n.1185+330_1185+331del
NM_015404.4:c.1166+330_1166+331del MANE Select	NP_056219.3:n.1166+330_1166+331del
NM_001173425.2:c.1166+330_1166+331del	NP_001166896.1:n.1166+330_1166+331del
NM_001083885.3:c.17+330_17+331del	NP_001077354.2:n.17+330_17+331del