Canonical Allele Identifier: CA2260641946

Gene: WNK4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787540_42787543delinsCTTG , CM000679.2:g.42787540_42787543delinsCTTG	GRCh38
NC_000017.10:g.40939558_40939561delinsCTTG , CM000679.1:g.40939558_40939561delinsCTTG	GRCh37
NC_000017.9:g.38193084_38193087delinsCTTG	NCBI36
NG_016227.1:g.11910_11913delinsCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1739_1741+1delinsCTTG
ENST00000246914.9:c.1739_1741+1delinsCTTG
ENST00000587705.5:n.419_421+1delinsCTTG
ENST00000591448.5:c.*240_*242+1delinsCTTG
ENST00000592072.1:n.419_421+1delinsCTTG
NM_032387.4:c.1739_1741+1delinsCTTG
XM_005257595.3:c.1739_1741+1delinsCTTG
XM_005257596.2:c.1739_1741+1delinsCTTG
XM_005257597.3:c.1739_1741+1delinsCTTG
XM_006722020.2:c.1739_1741+1delinsCTTG
XM_006722021.1:c.731_733+1delinsCTTG
XM_006722022.1:c.731_733+1delinsCTTG
XM_011525132.1:c.1739_1741+1delinsCTTG
XM_011525133.1:c.1739_1741+1delinsCTTG
XM_011525134.1:c.1739_1741+1delinsCTTG
XM_011525135.1:c.1739_1741+1delinsCTTG
NM_001321299.1:c.731_733+1delinsCTTG
XM_017024962.1:c.1739_1741+1delinsCTTG
XM_017024966.1:c.731_733+1delinsCTTG
NM_032387.5:c.1739_1741+1delinsCTTG
NM_001321299.2:c.731_733+1delinsCTTG