Canonical Allele Identifier: CA399656167

Gene: WNK4

Linked Data

• MyVariant Identifiers: chr17:g.40939320G>A (hg19) ; chr17:g.42787302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787302G>A , CM000679.2:g.42787302G>A	GRCh38
NC_000017.10:g.40939320G>A , CM000679.1:g.40939320G>A	GRCh37
NC_000017.9:g.38192846G>A	NCBI36
NG_016227.1:g.11672G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1501G>A MANE Select	ENSP00000246914.4:p.Ala501Thr
ENST00000246914.9:c.1501G>A	ENSP00000246914.4:p.Ala501Thr
ENST00000587705.5:n.181G>A
ENST00000591448.5:c.*2G>A	ENSP00000467088.1:n.*2G>A
ENST00000592072.1:n.181G>A
NM_032387.4:c.1501G>A	NP_115763.2:p.Ala501Thr
XM_005257595.3:c.1501G>A	XP_005257652.1:p.Ala501Thr
XM_005257596.2:c.1501G>A	XP_005257653.1:p.Ala501Thr
XM_005257597.3:c.1501G>A	XP_005257654.1:p.Ala501Thr
XM_006722020.2:c.1501G>A	XP_006722083.1:p.Ala501Thr
XM_006722021.1:c.493G>A	XP_006722084.1:p.Ala165Thr
XM_006722022.1:c.493G>A	XP_006722085.1:p.Ala165Thr
XM_011525132.1:c.1501G>A	XP_011523434.1:p.Ala501Thr
XM_011525133.1:c.1501G>A	XP_011523435.1:p.Ala501Thr
XM_011525134.1:c.1501G>A	XP_011523436.1:p.Ala501Thr
XM_011525135.1:c.1501G>A	XP_011523437.1:p.Ala501Thr
NM_001321299.1:c.493G>A	NP_001308228.1:p.Ala165Thr
XM_017024962.1:c.1501G>A	XP_016880451.1:p.Ala501Thr
XM_017024966.1:c.493G>A	XP_016880455.1:p.Ala165Thr
NM_032387.5:c.1501G>A MANE Select	NP_115763.2:p.Ala501Thr
NM_001321299.2:c.493G>A	NP_001308228.1:p.Ala165Thr