Canonical Allele Identifier: CA5205965

Gene: WHRN

Linked Data

• dbSNP Id: rs781539585
• ExAC: 9:117186582 TGAAGCCAGTTG / T
• gnomAD v2: 9-117186582-TGAAGCCAGTTG-T
• gnomAD v3: 9-114424302-TGAAGCCAGTTG-T
• gnomAD v4: 9-114424302-TGAAGCCAGTTG-T
• MyVariant Identifiers: chr9:g.117186583_117186593del (hg19) ; chr9:g.114424303_114424313del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114424304_114424314del , CM000671.2:g.114424304_114424314del	GRCh38
NC_000009.11:g.117186584_117186594del , CM000671.1:g.117186584_117186594del	GRCh37
NC_000009.10:g.116226405_116226415del	NCBI36
NG_016700.1:g.86144_86154del

Transcript Alleles

HGVS	Amino-acid change
ENST00000699486.1:c.1140+21_1140+31del	ENSP00000514397.1:n.1140+21_1140+31del
ENST00000362057.4:c.1416+21_1416+31del MANE Select	ENSP00000354623.3:n.1416+21_1416+31del
ENST00000673811.1:n.2350+21_2350+31del
ENST00000674036.8:c.599+21_599+31del
ENST00000674048.1:n.1297+21_1297+31del
ENST00000265134.10:c.267+21_267+31del	ENSP00000265134.6:n.267+21_267+31del
ENST00000362057.3:c.1416+21_1416+31del	ENSP00000354623.3:n.1416+21_1416+31del
ENST00000374059.7:c.363+21_363+31del	ENSP00000363172.3:n.363+21_363+31del
NM_001083885.2:c.267+21_267+31del	NP_001077354.2:n.267+21_267+31del
NM_001173425.1:c.1416+21_1416+31del	NP_001166896.1:n.1416+21_1416+31del
NM_015404.3:c.1416+21_1416+31del	NP_056219.3:n.1416+21_1416+31del
XM_005251897.3:c.964-16295_964-16285del	XP_005251954.2:n.964-16295_964-16285del
XM_011518484.1:c.1416+21_1416+31del	XP_011516786.1:n.1416+21_1416+31del
XM_011518485.1:c.1416+21_1416+31del	XP_011516787.1:n.1416+21_1416+31del
XM_011518486.1:c.1416+21_1416+31del	XP_011516788.1:n.1416+21_1416+31del
XM_011518487.1:c.1290+21_1290+31del	XP_011516789.1:n.1290+21_1290+31del
XM_011518488.1:c.1416+21_1416+31del	XP_011516790.1:n.1416+21_1416+31del
XM_011518489.1:c.1416+21_1416+31del	XP_011516791.1:n.1416+21_1416+31del
XM_011518490.1:c.1416+21_1416+31del	XP_011516792.1:n.1416+21_1416+31del
XM_011518491.1:c.1416+21_1416+31del	XP_011516793.1:n.1416+21_1416+31del
XM_011518492.1:c.1416+21_1416+31del	XP_011516794.1:n.1416+21_1416+31del
XM_011518493.1:c.1416+21_1416+31del	XP_011516795.1:n.1416+21_1416+31del
XM_011518494.1:c.1416+21_1416+31del	XP_011516796.1:n.1416+21_1416+31del
XM_011518495.1:c.93+21_93+31del	XP_011516797.1:n.93+21_93+31del
XR_929747.1:n.2124+21_2124+31del
XR_929748.1:n.2124+21_2124+31del
XR_929749.1:n.2124+21_2124+31del
XR_929750.1:n.2124+21_2124+31del
XR_929751.1:n.2124+21_2124+31del
XR_929752.1:n.2124+21_2124+31del
XR_929753.1:n.2124+21_2124+31del
XR_929754.1:n.2124+21_2124+31del
XR_929755.1:n.2124+21_2124+31del
XR_929756.1:n.2124+21_2124+31del
XR_929757.1:n.2124+21_2124+31del
NM_001346890.1:c.363+21_363+31del	NP_001333819.1:n.363+21_363+31del
XM_011518486.2:c.1416+21_1416+31del	XP_011516788.1:n.1416+21_1416+31del
XM_011518487.2:c.1290+21_1290+31del	XP_011516789.1:n.1290+21_1290+31del
XM_011518488.2:c.1416+21_1416+31del	XP_011516790.1:n.1416+21_1416+31del
XM_011518489.3:c.1416+21_1416+31del	XP_011516791.1:n.1416+21_1416+31del
XM_011518491.3:c.1416+21_1416+31del	XP_011516793.1:n.1416+21_1416+31del
XM_011518492.2:c.1416+21_1416+31del	XP_011516794.1:n.1416+21_1416+31del
XM_011518494.3:c.1416+21_1416+31del	XP_011516796.1:n.1416+21_1416+31del
XR_929747.2:n.1435+21_1435+31del
XR_929748.2:n.1435+21_1435+31del
XR_929749.2:n.1435+21_1435+31del
XR_929750.3:n.1435+21_1435+31del
XR_929752.2:n.1435+21_1435+31del
XR_929753.3:n.1435+21_1435+31del
XR_929754.2:n.1435+21_1435+31del
XR_929755.3:n.1435+21_1435+31del
XR_929756.2:n.1435+21_1435+31del
XR_929757.2:n.1435+21_1435+31del
NM_015404.4:c.1416+21_1416+31del MANE Select	NP_056219.3:n.1416+21_1416+31del
NM_001173425.2:c.1416+21_1416+31del	NP_001166896.1:n.1416+21_1416+31del
NM_001083885.3:c.267+21_267+31del	NP_001077354.2:n.267+21_267+31del