Canonical Allele Identifier: CA290785160

Gene: WNK4

Linked Data

• ClinVar Variation Id: 2314434
• ClinVar RCV Id: RCV002897375
• dbSNP Id: rs891599658
• MyVariant Identifiers: chr17:g.40939519A>G (hg19) ; chr17:g.42787501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787501A>G , CM000679.2:g.42787501A>G	GRCh38
NC_000017.10:g.40939519A>G , CM000679.1:g.40939519A>G	GRCh37
NC_000017.9:g.38193045A>G	NCBI36
NG_016227.1:g.11871A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1700A>G MANE Select	ENSP00000246914.4:p.Gln567Arg
ENST00000246914.9:c.1700A>G	ENSP00000246914.4:p.Gln567Arg
ENST00000587705.5:n.380A>G
ENST00000591448.5:c.*201A>G	ENSP00000467088.1:n.*201A>G
ENST00000592072.1:n.380A>G
NM_032387.4:c.1700A>G	NP_115763.2:p.Gln567Arg
XM_005257595.3:c.1700A>G	XP_005257652.1:p.Gln567Arg
XM_005257596.2:c.1700A>G	XP_005257653.1:p.Gln567Arg
XM_005257597.3:c.1700A>G	XP_005257654.1:p.Gln567Arg
XM_006722020.2:c.1700A>G	XP_006722083.1:p.Gln567Arg
XM_006722021.1:c.692A>G	XP_006722084.1:p.Gln231Arg
XM_006722022.1:c.692A>G	XP_006722085.1:p.Gln231Arg
XM_011525132.1:c.1700A>G	XP_011523434.1:p.Gln567Arg
XM_011525133.1:c.1700A>G	XP_011523435.1:p.Gln567Arg
XM_011525134.1:c.1700A>G	XP_011523436.1:p.Gln567Arg
XM_011525135.1:c.1700A>G	XP_011523437.1:p.Gln567Arg
NM_001321299.1:c.692A>G	NP_001308228.1:p.Gln231Arg
XM_017024962.1:c.1700A>G	XP_016880451.1:p.Gln567Arg
XM_017024966.1:c.692A>G	XP_016880455.1:p.Gln231Arg
NM_032387.5:c.1700A>G MANE Select	NP_115763.2:p.Gln567Arg
NM_001321299.2:c.692A>G	NP_001308228.1:p.Gln231Arg