Canonical Allele Identifier: CA2260641937

Gene: WNK4

Linked Data

• dbSNP Id: rs2054563528

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787518del , CM000679.2:g.42787518del	GRCh38
NC_000017.10:g.40939536del , CM000679.1:g.40939536del	GRCh37
NC_000017.9:g.38193062del	NCBI36
NG_016227.1:g.11888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1717del MANE Select	ENSP00000246914.4:p.His573ThrfsTer?
ENST00000246914.9:c.1717del	ENSP00000246914.4:p.His573ThrfsTer?
ENST00000587705.5:n.397del
ENST00000591448.5:c.*218del	ENSP00000467088.1:n.*218del
ENST00000592072.1:n.397del
NM_032387.4:c.1717del	NP_115763.2:p.His573ThrfsTer?
XM_005257595.3:c.1717del	XP_005257652.1:p.His573ThrfsTer?
XM_005257596.2:c.1717del	XP_005257653.1:p.His573ThrfsTer?
XM_005257597.3:c.1717del	XP_005257654.1:p.His573ThrfsTer?
XM_006722020.2:c.1717del	XP_006722083.1:p.His573ThrfsTer?
XM_006722021.1:c.709del	XP_006722084.1:p.His237ThrfsTer?
XM_006722022.1:c.709del	XP_006722085.1:p.His237ThrfsTer?
XM_011525132.1:c.1717del	XP_011523434.1:p.His573ThrfsTer?
XM_011525133.1:c.1717del	XP_011523435.1:p.His573ThrfsTer?
XM_011525134.1:c.1717del	XP_011523436.1:p.His573ThrfsTer?
XM_011525135.1:c.1717del	XP_011523437.1:p.His573ThrfsTer?
NM_001321299.1:c.709del	NP_001308228.1:p.His237ThrfsTer?
XM_017024962.1:c.1717del	XP_016880451.1:p.His573ThrfsTer?
XM_017024966.1:c.709del	XP_016880455.1:p.His237ThrfsTer?
NM_032387.5:c.1717del MANE Select	NP_115763.2:p.His573ThrfsTer?
NM_001321299.2:c.709del	NP_001308228.1:p.His237ThrfsTer?