Canonical Allele Identifier: CA290785066

Gene: WNK4

Linked Data

• dbSNP Id: rs895599804
• gnomAD v2: 17-40939422-C-T
• gnomAD v3: 17-42787404-C-T
• gnomAD v4: 17-42787404-C-T
• MyVariant Identifiers: chr17:g.40939422C>T (hg19) ; chr17:g.42787404C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787404C>T , CM000679.2:g.42787404C>T	GRCh38
NC_000017.10:g.40939422C>T , CM000679.1:g.40939422C>T	GRCh37
NC_000017.9:g.38192948C>T	NCBI36
NG_016227.1:g.11774C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000246914.10:c.1603C>T MANE Select	ENSP00000246914.4:p.Pro535Ser
ENST00000246914.9:c.1603C>T	ENSP00000246914.4:p.Pro535Ser
ENST00000587705.5:n.283C>T
ENST00000591448.5:c.*104C>T	ENSP00000467088.1:n.*104C>T
ENST00000592072.1:n.283C>T
NM_032387.4:c.1603C>T	NP_115763.2:p.Pro535Ser
XM_005257595.3:c.1603C>T	XP_005257652.1:p.Pro535Ser
XM_005257596.2:c.1603C>T	XP_005257653.1:p.Pro535Ser
XM_005257597.3:c.1603C>T	XP_005257654.1:p.Pro535Ser
XM_006722020.2:c.1603C>T	XP_006722083.1:p.Pro535Ser
XM_006722021.1:c.595C>T	XP_006722084.1:p.Pro199Ser
XM_006722022.1:c.595C>T	XP_006722085.1:p.Pro199Ser
XM_011525132.1:c.1603C>T	XP_011523434.1:p.Pro535Ser
XM_011525133.1:c.1603C>T	XP_011523435.1:p.Pro535Ser
XM_011525134.1:c.1603C>T	XP_011523436.1:p.Pro535Ser
XM_011525135.1:c.1603C>T	XP_011523437.1:p.Pro535Ser
NM_001321299.1:c.595C>T	NP_001308228.1:p.Pro199Ser
XM_017024962.1:c.1603C>T	XP_016880451.1:p.Pro535Ser
XM_017024966.1:c.595C>T	XP_016880455.1:p.Pro199Ser
NM_032387.5:c.1603C>T MANE Select	NP_115763.2:p.Pro535Ser
NM_001321299.2:c.595C>T	NP_001308228.1:p.Pro199Ser