Canonical Allele Identifier: CA8584056
Gene: WNK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2263544
ClinVar RCV Id: RCV002797979
dbSNP Id: rs374889836

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42787473C>T , CM000679.2:g.42787473C>T GRCh38
NC_000017.10:g.40939491C>T , CM000679.1:g.40939491C>T GRCh37
NC_000017.9:g.38193017C>T NCBI36
NG_016227.1:g.11843C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246914.10:c.1672C>T MANE Select ENSP00000246914.4:p.Pro558Ser
ENST00000246914.9:c.1672C>T ENSP00000246914.4:p.Pro558Ser
ENST00000587705.5:n.352C>T
ENST00000591448.5:c.*173C>T ENSP00000467088.1:n.*173C>T
ENST00000592072.1:n.352C>T
NM_032387.4:c.1672C>T NP_115763.2:p.Pro558Ser
XM_005257595.3:c.1672C>T XP_005257652.1:p.Pro558Ser
XM_005257596.2:c.1672C>T XP_005257653.1:p.Pro558Ser
XM_005257597.3:c.1672C>T XP_005257654.1:p.Pro558Ser
XM_006722020.2:c.1672C>T XP_006722083.1:p.Pro558Ser
XM_006722021.1:c.664C>T XP_006722084.1:p.Pro222Ser
XM_006722022.1:c.664C>T XP_006722085.1:p.Pro222Ser
XM_011525132.1:c.1672C>T XP_011523434.1:p.Pro558Ser
XM_011525133.1:c.1672C>T XP_011523435.1:p.Pro558Ser
XM_011525134.1:c.1672C>T XP_011523436.1:p.Pro558Ser
XM_011525135.1:c.1672C>T XP_011523437.1:p.Pro558Ser
NM_001321299.1:c.664C>T NP_001308228.1:p.Pro222Ser
XM_017024962.1:c.1672C>T XP_016880451.1:p.Pro558Ser
XM_017024966.1:c.664C>T XP_016880455.1:p.Pro222Ser
NM_032387.5:c.1672C>T MANE Select NP_115763.2:p.Pro558Ser
NM_001321299.2:c.664C>T NP_001308228.1:p.Pro222Ser