Canonical Allele Identifier: CA8584464

Gene: WNK4 COA3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42795326G>A , CM000679.2:g.42795326G>A	GRCh38
NC_000017.10:g.40947344G>A , CM000679.1:g.40947344G>A	GRCh37
NC_000017.9:g.38200870G>A	NCBI36
NG_016227.1:g.19696G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032387.5:c.2905G>A (WNK4) MANE Select	NP_115763.2:p.Val969Ile
ENST00000246914.10:c.2905G>A (WNK4) MANE Select	ENSP00000246914.4:p.Val969Ile
NM_001321299.1:c.1897G>A (WNK4)	NP_001308228.1:p.Val633Ile
NM_001321299.2:c.1897G>A (WNK4)	NP_001308228.1:p.Val633Ile
NM_032387.4:c.2905G>A (WNK4)	NP_115763.2:p.Val969Ile
ENST00000246914.9:c.2905G>A (WNK4)	ENSP00000246914.4:p.Val969Ile
ENST00000586680.1:c.*970C>T (COA3)	ENSP00000467546.1:n.*970C>T
ENST00000587745.1:c.71-299G>A (WNK4)	ENSP00000467312.1:n.71-299G>A
ENST00000591448.5:c.*1406G>A (WNK4)	ENSP00000467088.1:n.*1406G>A
XM_005257595.3:c.2905G>A (WNK4)	XP_005257652.1:p.Val969Ile
XM_005257596.2:c.2902G>A (WNK4)	XP_005257653.1:p.Val968Ile
XM_005257597.3:c.2905G>A (WNK4)	XP_005257654.1:p.Val969Ile
XM_006722020.2:c.2767G>A (WNK4)	XP_006722083.1:p.Val923Ile
XM_006722021.1:c.1897G>A (WNK4)	XP_006722084.1:p.Val633Ile
XM_006722022.1:c.1897G>A (WNK4)	XP_006722085.1:p.Val633Ile
XM_011525132.1:c.2902G>A (WNK4)	XP_011523434.1:p.Val968Ile
XM_011525133.1:c.2905G>A (WNK4)	XP_011523435.1:p.Val969Ile
XM_011525134.1:c.2764G>A (WNK4)	XP_011523436.1:p.Val922Ile
XM_011525135.1:c.2905G>A (WNK4)	XP_011523437.1:p.Val969Ile
XM_017024962.1:c.2905G>A (WNK4)	XP_016880451.1:p.Val969Ile
XM_017024966.1:c.1897G>A (WNK4)	XP_016880455.1:p.Val633Ile