Canonical Allele Identifier: CA772148388
Gene: WNK4 HGNC NCBI

Linked Data

dbSNP Id: rs1358019662

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42787169_42787172del , CM000679.2:g.42787169_42787172del GRCh38
NC_000017.10:g.40939187_40939190del , CM000679.1:g.40939187_40939190del GRCh37
NC_000017.9:g.38192713_38192716del NCBI36
NG_016227.1:g.11539_11542del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246914.10:c.1477-109_1477-106del MANE Select ENSP00000246914.4:n.1477-109_1477-106del
ENST00000246914.9:c.1477-109_1477-106del ENSP00000246914.4:n.1477-109_1477-106del
ENST00000587705.5:n.157-109_157-106del
ENST00000591448.5:c.1388-109_1388-106del ENSP00000467088.1:n.1388-109_1388-106del
ENST00000592072.1:n.157-109_157-106del
NM_032387.4:c.1477-109_1477-106del NP_115763.2:n.1477-109_1477-106del
XM_005257595.3:c.1477-109_1477-106del XP_005257652.1:n.1477-109_1477-106del
XM_005257596.2:c.1477-109_1477-106del XP_005257653.1:n.1477-109_1477-106del
XM_005257597.3:c.1477-109_1477-106del XP_005257654.1:n.1477-109_1477-106del
XM_006722020.2:c.1477-109_1477-106del XP_006722083.1:n.1477-109_1477-106del
XM_006722021.1:c.469-109_469-106del XP_006722084.1:n.469-109_469-106del
XM_006722022.1:c.469-109_469-106del XP_006722085.1:n.469-109_469-106del
XM_011525132.1:c.1477-109_1477-106del XP_011523434.1:n.1477-109_1477-106del
XM_011525133.1:c.1477-109_1477-106del XP_011523435.1:n.1477-109_1477-106del
XM_011525134.1:c.1477-109_1477-106del XP_011523436.1:n.1477-109_1477-106del
XM_011525135.1:c.1477-109_1477-106del XP_011523437.1:n.1477-109_1477-106del
NM_001321299.1:c.469-109_469-106del NP_001308228.1:n.469-109_469-106del
XM_017024962.1:c.1477-109_1477-106del XP_016880451.1:n.1477-109_1477-106del
XM_017024966.1:c.469-109_469-106del XP_016880455.1:n.469-109_469-106del
NM_032387.5:c.1477-109_1477-106del MANE Select NP_115763.2:n.1477-109_1477-106del
NM_001321299.2:c.469-109_469-106del NP_001308228.1:n.469-109_469-106del