Canonical Allele Identifier: CA2638017114

Gene: WNK4

Linked Data

• gnomAD v4: 17-42787448-T-TGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787448_42787449insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000679.2:g.42787448_42787449insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000017.10:g.40939466_40939467insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000679.1:g.40939466_40939467insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000017.9:g.38192992_38192993insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_016227.1:g.11818_11819insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000246914.4:p.Pro550GlyfsTer22
ENST00000246914.9:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000246914.4:p.Pro550GlyfsTer22
ENST00000587705.5:n.327_328insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000591448.5:c.*148_*149insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000467088.1:n.*148_*149insGGGGGGGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000592072.1:n.327_328insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_032387.4:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	NP_115763.2:p.Pro550GlyfsTer22
XM_005257595.3:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_005257652.1:p.Pro550GlyfsTer22
XM_005257596.2:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_005257653.1:p.Pro550GlyfsTer22
XM_005257597.3:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_005257654.1:p.Pro550GlyfsTer22
XM_006722020.2:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_006722083.1:p.Pro550GlyfsTer22
XM_006722021.1:c.639_640insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_006722084.1:p.Pro214GlyfsTer22
XM_006722022.1:c.639_640insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_006722085.1:p.Pro214GlyfsTer22
XM_011525132.1:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_011523434.1:p.Pro550GlyfsTer22
XM_011525133.1:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_011523435.1:p.Pro550GlyfsTer22
XM_011525134.1:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_011523436.1:p.Pro550GlyfsTer22
XM_011525135.1:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_011523437.1:p.Pro550GlyfsTer22
NM_001321299.1:c.639_640insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	NP_001308228.1:p.Pro214GlyfsTer22
XM_017024962.1:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_016880451.1:p.Pro550GlyfsTer22
XM_017024966.1:c.639_640insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	XP_016880455.1:p.Pro214GlyfsTer22
NM_032387.5:c.1647_1648insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_115763.2:p.Pro550GlyfsTer22
NM_001321299.2:c.639_640insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	NP_001308228.1:p.Pro214GlyfsTer22