Canonical Allele Identifier: CA8584345

Gene: WNK4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42794615A>G , CM000679.2:g.42794615A>G	GRCh38
NC_000017.10:g.40946633A>G , CM000679.1:g.40946633A>G	GRCh37
NC_000017.9:g.38200159A>G	NCBI36
NG_016227.1:g.18985A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032387.5:c.2297A>G MANE Select	NP_115763.2:p.Glu766Gly
ENST00000246914.10:c.2297A>G MANE Select	ENSP00000246914.4:p.Glu766Gly
NM_001321299.1:c.1289A>G	NP_001308228.1:p.Glu430Gly
NM_001321299.2:c.1289A>G	NP_001308228.1:p.Glu430Gly
NM_032387.4:c.2297A>G	NP_115763.2:p.Glu766Gly
ENST00000246914.9:c.2297A>G	ENSP00000246914.4:p.Glu766Gly
ENST00000587745.1:c.17A>G	ENSP00000467312.1:p.Glu6Gly
ENST00000591448.5:c.*798A>G	ENSP00000467088.1:n.*798A>G
XM_005257595.3:c.2297A>G	XP_005257652.1:p.Glu766Gly
XM_005257596.2:c.2297A>G	XP_005257653.1:p.Glu766Gly
XM_005257597.3:c.2297A>G	XP_005257654.1:p.Glu766Gly
XM_006722020.2:c.2159A>G	XP_006722083.1:p.Glu720Gly
XM_006722021.1:c.1289A>G	XP_006722084.1:p.Glu430Gly
XM_006722022.1:c.1289A>G	XP_006722085.1:p.Glu430Gly
XM_011525132.1:c.2297A>G	XP_011523434.1:p.Glu766Gly
XM_011525133.1:c.2297A>G	XP_011523435.1:p.Glu766Gly
XM_011525134.1:c.2159A>G	XP_011523436.1:p.Glu720Gly
XM_011525135.1:c.2297A>G	XP_011523437.1:p.Glu766Gly
XM_017024962.1:c.2297A>G	XP_016880451.1:p.Glu766Gly
XM_017024966.1:c.1289A>G	XP_016880455.1:p.Glu430Gly