Canonical Allele Identifier: CA626220172

Gene: WNK4

Linked Data

• dbSNP Id: rs1201173960
• gnomAD v2: 17-40939289-A-G
• gnomAD v4: 17-42787271-A-G
• MyVariant Identifiers: chr17:g.40939289A>G (hg19) ; chr17:g.42787271A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787271A>G , CM000679.2:g.42787271A>G	GRCh38
NC_000017.10:g.40939289A>G , CM000679.1:g.40939289A>G	GRCh37
NC_000017.9:g.38192815A>G	NCBI36
NG_016227.1:g.11641A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1477-7A>G MANE Select	ENSP00000246914.4:n.1477-7A>G
ENST00000246914.9:c.1477-7A>G	ENSP00000246914.4:n.1477-7A>G
ENST00000587705.5:n.157-7A>G
ENST00000591448.5:c.1388-7A>G	ENSP00000467088.1:n.1388-7A>G
ENST00000592072.1:n.157-7A>G
NM_032387.4:c.1477-7A>G	NP_115763.2:n.1477-7A>G
XM_005257595.3:c.1477-7A>G	XP_005257652.1:n.1477-7A>G
XM_005257596.2:c.1477-7A>G	XP_005257653.1:n.1477-7A>G
XM_005257597.3:c.1477-7A>G	XP_005257654.1:n.1477-7A>G
XM_006722020.2:c.1477-7A>G	XP_006722083.1:n.1477-7A>G
XM_006722021.1:c.469-7A>G	XP_006722084.1:n.469-7A>G
XM_006722022.1:c.469-7A>G	XP_006722085.1:n.469-7A>G
XM_011525132.1:c.1477-7A>G	XP_011523434.1:n.1477-7A>G
XM_011525133.1:c.1477-7A>G	XP_011523435.1:n.1477-7A>G
XM_011525134.1:c.1477-7A>G	XP_011523436.1:n.1477-7A>G
XM_011525135.1:c.1477-7A>G	XP_011523437.1:n.1477-7A>G
NM_001321299.1:c.469-7A>G	NP_001308228.1:n.469-7A>G
XM_017024962.1:c.1477-7A>G	XP_016880451.1:n.1477-7A>G
XM_017024966.1:c.469-7A>G	XP_016880455.1:n.469-7A>G
NM_032387.5:c.1477-7A>G MANE Select	NP_115763.2:n.1477-7A>G
NM_001321299.2:c.469-7A>G	NP_001308228.1:n.469-7A>G