Canonical Allele Identifier: CA2733784887

Gene: WNK4

Linked Data

• dbSNP Id: rs2144033860

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787440_42787441insGGGGGGGGGGGGGGGGGGGGGG , CM000679.2:g.42787440_42787441insGGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000017.10:g.40939458_40939459insGGGGGGGGGGGGGGGGGGGGGG , CM000679.1:g.40939458_40939459insGGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000017.9:g.38192984_38192985insGGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_016227.1:g.11810_11811insGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000246914.4:p.Ala547GlyfsTer18
ENST00000246914.9:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	ENSP00000246914.4:p.Ala547GlyfsTer18
ENST00000587705.5:n.319_320insGGGGGGGGGGGGGGGGGGGGGG
ENST00000591448.5:c.*140_*141insGGGGGGGGGGGGGGGGGGGGGG	ENSP00000467088.1:n.*140_*141insGGGGGGGGGGGGGGGGGGGGGG
ENST00000592072.1:n.319_320insGGGGGGGGGGGGGGGGGGGGGG
NM_032387.4:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	NP_115763.2:p.Ala547GlyfsTer18
XM_005257595.3:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_005257652.1:p.Ala547GlyfsTer18
XM_005257596.2:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_005257653.1:p.Ala547GlyfsTer18
XM_005257597.3:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_005257654.1:p.Ala547GlyfsTer18
XM_006722020.2:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_006722083.1:p.Ala547GlyfsTer18
XM_006722021.1:c.631_632insGGGGGGGGGGGGGGGGGGGGGG	XP_006722084.1:p.Ala211GlyfsTer18
XM_006722022.1:c.631_632insGGGGGGGGGGGGGGGGGGGGGG	XP_006722085.1:p.Ala211GlyfsTer18
XM_011525132.1:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_011523434.1:p.Ala547GlyfsTer18
XM_011525133.1:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_011523435.1:p.Ala547GlyfsTer18
XM_011525134.1:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_011523436.1:p.Ala547GlyfsTer18
XM_011525135.1:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_011523437.1:p.Ala547GlyfsTer18
NM_001321299.1:c.631_632insGGGGGGGGGGGGGGGGGGGGGG	NP_001308228.1:p.Ala211GlyfsTer18
XM_017024962.1:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG	XP_016880451.1:p.Ala547GlyfsTer18
XM_017024966.1:c.631_632insGGGGGGGGGGGGGGGGGGGGGG	XP_016880455.1:p.Ala211GlyfsTer18
NM_032387.5:c.1639_1640insGGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_115763.2:p.Ala547GlyfsTer18
NM_001321299.2:c.631_632insGGGGGGGGGGGGGGGGGGGGGG	NP_001308228.1:p.Ala211GlyfsTer18