Canonical Allele Identifier: CA8584065

Gene: WNK4

Linked Data

• dbSNP Id: rs777253974
• ExAC: 17:40939558 CTTG / C
• gnomAD v2: 17-40939558-CTTG-C
• gnomAD v4: 17-42787540-CTTG-C
• MyVariant Identifiers: chr17:g.40939559_40939561del (hg19) ; chr17:g.42787541_42787543del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787542_42787544del , CM000679.2:g.42787542_42787544del	GRCh38
NC_000017.10:g.40939560_40939562del , CM000679.1:g.40939560_40939562del	GRCh37
NC_000017.9:g.38193086_38193088del	NCBI36
NG_016227.1:g.11912_11914del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1741_1741+2del
ENST00000246914.9:c.1741_1741+2del
ENST00000587705.5:n.421_421+2del
ENST00000591448.5:c.*242_*242+2del
ENST00000592072.1:n.421_421+2del
NM_032387.4:c.1741_1741+2del
XM_005257595.3:c.1741_1741+2del
XM_005257596.2:c.1741_1741+2del
XM_005257597.3:c.1741_1741+2del
XM_006722020.2:c.1741_1741+2del
XM_006722021.1:c.733_733+2del
XM_006722022.1:c.733_733+2del
XM_011525132.1:c.1741_1741+2del
XM_011525133.1:c.1741_1741+2del
XM_011525134.1:c.1741_1741+2del
XM_011525135.1:c.1741_1741+2del
NM_001321299.1:c.733_733+2del
XM_017024962.1:c.1741_1741+2del
XM_017024966.1:c.733_733+2del
NM_032387.5:c.1741_1741+2del
NM_001321299.2:c.733_733+2del