Canonical Allele Identifier: CA2691374245

Gene: WHRN

Linked Data

• gnomAD v4: 9-114425871-TCTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114425879_114425882del , CM000671.2:g.114425879_114425882del	GRCh38
NC_000009.11:g.117188159_117188162del , CM000671.1:g.117188159_117188162del	GRCh37
NC_000009.10:g.116227980_116227983del	NCBI36
NG_016700.1:g.84582_84585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.890+336_890+339del	ENSP00000514397.1:n.890+336_890+339del
ENST00000362057.4:c.1166+336_1166+339del MANE Select	ENSP00000354623.3:n.1166+336_1166+339del
ENST00000673811.1:n.1250_1253del
ENST00000674036.8:c.349+336_349+339del
ENST00000674048.1:n.197_200del
ENST00000265134.10:c.17+336_17+339del	ENSP00000265134.6:n.17+336_17+339del
ENST00000362057.3:c.1166+336_1166+339del	ENSP00000354623.3:n.1166+336_1166+339del
ENST00000374059.7:c.-738_-735del	ENSP00000363172.3:n.-738_-735del
NM_001083885.2:c.17+336_17+339del	NP_001077354.2:n.17+336_17+339del
NM_001173425.1:c.1166+336_1166+339del	NP_001166896.1:n.1166+336_1166+339del
NM_015404.3:c.1166+336_1166+339del	NP_056219.3:n.1166+336_1166+339del
XM_005251897.3:c.964-17857_964-17854del	XP_005251954.2:n.964-17857_964-17854del
XM_011518484.1:c.1166+336_1166+339del	XP_011516786.1:n.1166+336_1166+339del
XM_011518485.1:c.1166+336_1166+339del	XP_011516787.1:n.1166+336_1166+339del
XM_011518486.1:c.1166+336_1166+339del	XP_011516788.1:n.1166+336_1166+339del
XM_011518487.1:c.1040+336_1040+339del	XP_011516789.1:n.1040+336_1040+339del
XM_011518488.1:c.1166+336_1166+339del	XP_011516790.1:n.1166+336_1166+339del
XM_011518489.1:c.1166+336_1166+339del	XP_011516791.1:n.1166+336_1166+339del
XM_011518490.1:c.1166+336_1166+339del	XP_011516792.1:n.1166+336_1166+339del
XM_011518491.1:c.1166+336_1166+339del	XP_011516793.1:n.1166+336_1166+339del
XM_011518492.1:c.1166+336_1166+339del	XP_011516794.1:n.1166+336_1166+339del
XM_011518493.1:c.1166+336_1166+339del	XP_011516795.1:n.1166+336_1166+339del
XM_011518494.1:c.1166+336_1166+339del	XP_011516796.1:n.1166+336_1166+339del
XM_011518495.1:c.-157-851_-157-848del	XP_011516797.1:n.-157-851_-157-848del
XR_929747.1:n.1874+336_1874+339del
XR_929748.1:n.1874+336_1874+339del
XR_929749.1:n.1874+336_1874+339del
XR_929750.1:n.1874+336_1874+339del
XR_929751.1:n.1874+336_1874+339del
XR_929752.1:n.1874+336_1874+339del
XR_929753.1:n.1874+336_1874+339del
XR_929754.1:n.1874+336_1874+339del
XR_929755.1:n.1874+336_1874+339del
XR_929756.1:n.1874+336_1874+339del
XR_929757.1:n.1874+336_1874+339del
NM_001346890.1:c.-738_-735del	NP_001333819.1:n.-738_-735del
XM_011518486.2:c.1166+336_1166+339del	XP_011516788.1:n.1166+336_1166+339del
XM_011518487.2:c.1040+336_1040+339del	XP_011516789.1:n.1040+336_1040+339del
XM_011518488.2:c.1166+336_1166+339del	XP_011516790.1:n.1166+336_1166+339del
XM_011518489.3:c.1166+336_1166+339del	XP_011516791.1:n.1166+336_1166+339del
XM_011518491.3:c.1166+336_1166+339del	XP_011516793.1:n.1166+336_1166+339del
XM_011518492.2:c.1166+336_1166+339del	XP_011516794.1:n.1166+336_1166+339del
XM_011518494.3:c.1166+336_1166+339del	XP_011516796.1:n.1166+336_1166+339del
XR_929747.2:n.1185+336_1185+339del
XR_929748.2:n.1185+336_1185+339del
XR_929749.2:n.1185+336_1185+339del
XR_929750.3:n.1185+336_1185+339del
XR_929752.2:n.1185+336_1185+339del
XR_929753.3:n.1185+336_1185+339del
XR_929754.2:n.1185+336_1185+339del
XR_929755.3:n.1185+336_1185+339del
XR_929756.2:n.1185+336_1185+339del
XR_929757.2:n.1185+336_1185+339del
NM_015404.4:c.1166+336_1166+339del MANE Select	NP_056219.3:n.1166+336_1166+339del
NM_001173425.2:c.1166+336_1166+339del	NP_001166896.1:n.1166+336_1166+339del
NM_001083885.3:c.17+336_17+339del	NP_001077354.2:n.17+336_17+339del