Canonical Allele Identifier: CA254225
Gene: WNK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7660
ClinVar RCV Id: RCV000008099
dbSNP Id: rs137853092
MyVariant Identifiers: chr17:g.40939512C>G (hg19) chr17:g.42787494C>G (hg38)
PubMed: PMID:718348 PMID:9171836 PMID:11498583 PMID:12107233 PMID:15292344 PMID:22073419
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42787494C>G , CM000679.2:g.42787494C>G GRCh38
NC_000017.10:g.40939512C>G , CM000679.1:g.40939512C>G GRCh37
NC_000017.9:g.38193038C>G NCBI36
NG_016227.1:g.11864C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000246914.10:c.1693C>G MANE Select ENSP00000246914.4:p.Gln565Glu
ENST00000246914.9:c.1693C>G ENSP00000246914.4:p.Gln565Glu
ENST00000587705.5:n.373C>G
ENST00000591448.5:c.*194C>G ENSP00000467088.1:n.*194C>G
ENST00000592072.1:n.373C>G
NM_032387.4:c.1693C>G NP_115763.2:p.Gln565Glu
XM_005257595.3:c.1693C>G XP_005257652.1:p.Gln565Glu
XM_005257596.2:c.1693C>G XP_005257653.1:p.Gln565Glu
XM_005257597.3:c.1693C>G XP_005257654.1:p.Gln565Glu
XM_006722020.2:c.1693C>G XP_006722083.1:p.Gln565Glu
XM_006722021.1:c.685C>G XP_006722084.1:p.Gln229Glu
XM_006722022.1:c.685C>G XP_006722085.1:p.Gln229Glu
XM_011525132.1:c.1693C>G XP_011523434.1:p.Gln565Glu
XM_011525133.1:c.1693C>G XP_011523435.1:p.Gln565Glu
XM_011525134.1:c.1693C>G XP_011523436.1:p.Gln565Glu
XM_011525135.1:c.1693C>G XP_011523437.1:p.Gln565Glu
NM_001321299.1:c.685C>G NP_001308228.1:p.Gln229Glu
XM_017024962.1:c.1693C>G XP_016880451.1:p.Gln565Glu
XM_017024966.1:c.685C>G XP_016880455.1:p.Gln229Glu
NM_032387.5:c.1693C>G MANE Select NP_115763.2:p.Gln565Glu
NM_001321299.2:c.685C>G NP_001308228.1:p.Gln229Glu
Search 100 bp 5'
Search 100 bp 3'