Canonical Allele Identifier: CA590500376

Gene: WHRN

Linked Data

• dbSNP Id: rs1363790433
• gnomAD v2: 9-117165257-AG-A
• gnomAD v4: 9-114402977-AG-A
• MyVariant Identifiers: chr9:g.117165258del (hg19) ; chr9:g.114402978del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402978del , CM000671.2:g.114402978del	GRCh38
NC_000009.11:g.117165258del , CM000671.1:g.117165258del	GRCh37
NC_000009.10:g.116205079del	NCBI36
NG_016700.1:g.107479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.886-42del	ENSP00000514396.1:n.886-42del
ENST00000362057.4:c.2542-42del MANE Select	ENSP00000354623.3:n.2542-42del
ENST00000674036.8:c.1515-42del
ENST00000674048.1:n.2423-42del
ENST00000265134.10:c.1393-42del	ENSP00000265134.6:n.1393-42del
ENST00000362057.3:c.2542-42del	ENSP00000354623.3:n.2542-42del
ENST00000374059.7:c.1489-42del	ENSP00000363172.3:n.1489-42del
NM_001083885.2:c.1393-42del	NP_001077354.2:n.1393-42del
NM_001173425.1:c.2539-42del	NP_001166896.1:n.2539-42del
NM_015404.3:c.2542-42del	NP_056219.3:n.2542-42del
XM_005251897.3:c.1879-42del	XP_005251954.2:n.1879-42del
XM_011518484.1:c.2575-42del	XP_011516786.1:n.2575-42del
XM_011518485.1:c.2575-42del	XP_011516787.1:n.2575-42del
XM_011518486.1:c.2572-42del	XP_011516788.1:n.2572-42del
XM_011518487.1:c.2449-42del	XP_011516789.1:n.2449-42del
XM_011518488.1:c.2332-42del	XP_011516790.1:n.2332-42del
XM_011518495.1:c.1252-42del	XP_011516797.1:n.1252-42del
XR_929747.1:n.3479-42del
XR_929748.1:n.3377-42del
NM_001346890.1:c.1489-42del	NP_001333819.1:n.1489-42del
XM_011518486.2:c.2572-42del	XP_011516788.1:n.2572-42del
XM_011518487.2:c.2449-42del	XP_011516789.1:n.2449-42del
XM_011518488.2:c.2332-42del	XP_011516790.1:n.2332-42del
XR_929747.2:n.2790-42del
XR_929748.2:n.2688-42del
NM_015404.4:c.2542-42del MANE Select	NP_056219.3:n.2542-42del
NM_001173425.2:c.2539-42del	NP_001166896.1:n.2539-42del
NM_001083885.3:c.1393-42del	NP_001077354.2:n.1393-42del