Canonical Allele Identifier: CA198648839

Gene: WHRN

Linked Data

• dbSNP Id: rs139155973
• gnomAD v3: 9-114403090-GGT-G
• gnomAD v4: 9-114403090-GGT-G
• MyVariant Identifiers: chr9:g.117165371_117165372del (hg19) ; chr9:g.114403091_114403092del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114403092_114403093del , CM000671.2:g.114403092_114403093del	GRCh38
NC_000009.11:g.117165372_117165373del , CM000671.1:g.117165372_117165373del	GRCh37
NC_000009.10:g.116205193_116205194del	NCBI36
NG_016700.1:g.107365_107366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.885+125_885+126del	ENSP00000514396.1:n.885+125_885+126del
ENST00000362057.4:c.2541+125_2541+126del MANE Select	ENSP00000354623.3:n.2541+125_2541+126del
ENST00000674036.8:c.1514+125_1514+126del
ENST00000674048.1:n.2422+125_2422+126del
ENST00000265134.10:c.1392+125_1392+126del	ENSP00000265134.6:n.1392+125_1392+126del
ENST00000362057.3:c.2541+125_2541+126del	ENSP00000354623.3:n.2541+125_2541+126del
ENST00000374059.7:c.1488+125_1488+126del	ENSP00000363172.3:n.1488+125_1488+126del
NM_001083885.2:c.1392+125_1392+126del	NP_001077354.2:n.1392+125_1392+126del
NM_001173425.1:c.2538+125_2538+126del	NP_001166896.1:n.2538+125_2538+126del
NM_015404.3:c.2541+125_2541+126del	NP_056219.3:n.2541+125_2541+126del
XM_005251897.3:c.1878+125_1878+126del	XP_005251954.2:n.1878+125_1878+126del
XM_011518484.1:c.2574+125_2574+126del	XP_011516786.1:n.2574+125_2574+126del
XM_011518485.1:c.2574+125_2574+126del	XP_011516787.1:n.2574+125_2574+126del
XM_011518486.1:c.2571+125_2571+126del	XP_011516788.1:n.2571+125_2571+126del
XM_011518487.1:c.2448+125_2448+126del	XP_011516789.1:n.2448+125_2448+126del
XM_011518488.1:c.2331+125_2331+126del	XP_011516790.1:n.2331+125_2331+126del
XM_011518495.1:c.1251+125_1251+126del	XP_011516797.1:n.1251+125_1251+126del
XR_929747.1:n.3478+125_3478+126del
XR_929748.1:n.3376+125_3376+126del
NM_001346890.1:c.1488+125_1488+126del	NP_001333819.1:n.1488+125_1488+126del
XM_011518486.2:c.2571+125_2571+126del	XP_011516788.1:n.2571+125_2571+126del
XM_011518487.2:c.2448+125_2448+126del	XP_011516789.1:n.2448+125_2448+126del
XM_011518488.2:c.2331+125_2331+126del	XP_011516790.1:n.2331+125_2331+126del
XR_929747.2:n.2789+125_2789+126del
XR_929748.2:n.2687+125_2687+126del
NM_015404.4:c.2541+125_2541+126del MANE Select	NP_056219.3:n.2541+125_2541+126del
NM_001173425.2:c.2538+125_2538+126del	NP_001166896.1:n.2538+125_2538+126del
NM_001083885.3:c.1392+125_1392+126del	NP_001077354.2:n.1392+125_1392+126del