Canonical Allele Identifier: CA2260641931

Gene: WNK4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787506T= , CM000679.2:g.42787506T=	GRCh38
NC_000017.10:g.40939524T= , CM000679.1:g.40939524T=	GRCh37
NC_000017.9:g.38193050T=	NCBI36
NG_016227.1:g.11876T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1705T= MANE Select	ENSP00000246914.4:p.Phe569=
ENST00000246914.9:c.1705T=	ENSP00000246914.4:p.Phe569=
ENST00000587705.5:n.385T=
ENST00000591448.5:c.*206T=	ENSP00000467088.1:n.*206T=
ENST00000592072.1:n.385T=
NM_032387.4:c.1705T=	NP_115763.2:p.Phe569=
XM_005257595.3:c.1705T=	XP_005257652.1:p.Phe569=
XM_005257596.2:c.1705T=	XP_005257653.1:p.Phe569=
XM_005257597.3:c.1705T=	XP_005257654.1:p.Phe569=
XM_006722020.2:c.1705T=	XP_006722083.1:p.Phe569=
XM_006722021.1:c.697T=	XP_006722084.1:p.Phe233=
XM_006722022.1:c.697T=	XP_006722085.1:p.Phe233=
XM_011525132.1:c.1705T=	XP_011523434.1:p.Phe569=
XM_011525133.1:c.1705T=	XP_011523435.1:p.Phe569=
XM_011525134.1:c.1705T=	XP_011523436.1:p.Phe569=
XM_011525135.1:c.1705T=	XP_011523437.1:p.Phe569=
NM_001321299.1:c.697T=	NP_001308228.1:p.Phe233=
XM_017024962.1:c.1705T=	XP_016880451.1:p.Phe569=
XM_017024966.1:c.697T=	XP_016880455.1:p.Phe233=
NM_032387.5:c.1705T= MANE Select	NP_115763.2:p.Phe569=
NM_001321299.2:c.697T=	NP_001308228.1:p.Phe233=