Canonical Allele Identifier: CA2260641952

Gene: WNK4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787554_42787555delinsCT , CM000679.2:g.42787554_42787555delinsCT	GRCh38
NC_000017.10:g.40939572_40939573delinsCT , CM000679.1:g.40939572_40939573delinsCT	GRCh37
NC_000017.9:g.38193098_38193099delinsCT	NCBI36
NG_016227.1:g.11924_11925delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1741+12_1741+13delinsCT MANE Select	ENSP00000246914.4:n.1741+12_1741+13delinsCT
ENST00000246914.9:c.1741+12_1741+13delinsCT	ENSP00000246914.4:n.1741+12_1741+13delinsCT
ENST00000587705.5:n.421+12_421+13delinsCT
ENST00000591448.5:c.*242+12_*242+13delinsCT	ENSP00000467088.1:n.*242+12_*242+13delinsCT
ENST00000592072.1:n.421+12_421+13delinsCT
NM_032387.4:c.1741+12_1741+13delinsCT	NP_115763.2:n.1741+12_1741+13delinsCT
XM_005257595.3:c.1741+12_1741+13delinsCT	XP_005257652.1:n.1741+12_1741+13delinsCT
XM_005257596.2:c.1741+12_1741+13delinsCT	XP_005257653.1:n.1741+12_1741+13delinsCT
XM_005257597.3:c.1741+12_1741+13delinsCT	XP_005257654.1:n.1741+12_1741+13delinsCT
XM_006722020.2:c.1741+12_1741+13delinsCT	XP_006722083.1:n.1741+12_1741+13delinsCT
XM_006722021.1:c.733+12_733+13delinsCT	XP_006722084.1:n.733+12_733+13delinsCT
XM_006722022.1:c.733+12_733+13delinsCT	XP_006722085.1:n.733+12_733+13delinsCT
XM_011525132.1:c.1741+12_1741+13delinsCT	XP_011523434.1:n.1741+12_1741+13delinsCT
XM_011525133.1:c.1741+12_1741+13delinsCT	XP_011523435.1:n.1741+12_1741+13delinsCT
XM_011525134.1:c.1741+12_1741+13delinsCT	XP_011523436.1:n.1741+12_1741+13delinsCT
XM_011525135.1:c.1741+12_1741+13delinsCT	XP_011523437.1:n.1741+12_1741+13delinsCT
NM_001321299.1:c.733+12_733+13delinsCT	NP_001308228.1:n.733+12_733+13delinsCT
XM_017024962.1:c.1741+12_1741+13delinsCT	XP_016880451.1:n.1741+12_1741+13delinsCT
XM_017024966.1:c.733+12_733+13delinsCT	XP_016880455.1:n.733+12_733+13delinsCT
NM_032387.5:c.1741+12_1741+13delinsCT MANE Select	NP_115763.2:n.1741+12_1741+13delinsCT
NM_001321299.2:c.733+12_733+13delinsCT	NP_001308228.1:n.733+12_733+13delinsCT