Canonical Allele Identifier: CA216476
Community Standard Title: NM_032387.5(WNK4):c.1323A>T (p.Glu441Asp)
Gene: WNK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42785329A>T , CM000679.2:g.42785329A>T GRCh38
NC_000017.10:g.40937347A>T , CM000679.1:g.40937347A>T GRCh37
NC_000017.9:g.38190873A>T NCBI36
NG_016227.1:g.9699A>T

Transcript Alleles

HGVS Amino-acid Change
NM_032387.5:c.1323A>T MANE Select NP_115763.2:p.Glu441Asp
ENST00000246914.10:c.1323A>T MANE Select ENSP00000246914.4:p.Glu441Asp
NM_001321299.1:c.315A>T NP_001308228.1:p.Glu105Asp
NM_001321299.2:c.315A>T NP_001308228.1:p.Glu105Asp
NM_032387.4:c.1323A>T NP_115763.2:p.Glu441Asp
ENST00000246914.9:c.1323A>T ENSP00000246914.4:p.Glu441Asp
ENST00000587705.5:n.3A>T
ENST00000591448.5:c.1234A>T ENSP00000467088.1:p.Thr412Ser
ENST00000592072.1:n.3A>T
XM_005257595.3:c.1323A>T XP_005257652.1:p.Glu441Asp
XM_005257596.2:c.1323A>T XP_005257653.1:p.Glu441Asp
XM_005257597.3:c.1323A>T XP_005257654.1:p.Glu441Asp
XM_006722020.2:c.1323A>T XP_006722083.1:p.Glu441Asp
XM_006722021.1:c.315A>T XP_006722084.1:p.Glu105Asp
XM_006722022.1:c.315A>T XP_006722085.1:p.Glu105Asp
XM_011525132.1:c.1323A>T XP_011523434.1:p.Glu441Asp
XM_011525133.1:c.1323A>T XP_011523435.1:p.Glu441Asp
XM_011525134.1:c.1323A>T XP_011523436.1:p.Glu441Asp
XM_011525135.1:c.1323A>T XP_011523437.1:p.Glu441Asp
XM_017024962.1:c.1323A>T XP_016880451.1:p.Glu441Asp
XM_017024966.1:c.315A>T XP_016880455.1:p.Glu105Asp