Canonical Allele Identifier: CA399656116

Gene: WNK4

Linked Data

• gnomAD v4: 17-42787294-T-C
• MyVariant Identifiers: chr17:g.40939312T>C (hg19) ; chr17:g.42787294T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787294T>C , CM000679.2:g.42787294T>C	GRCh38
NC_000017.10:g.40939312T>C , CM000679.1:g.40939312T>C	GRCh37
NC_000017.9:g.38192838T>C	NCBI36
NG_016227.1:g.11664T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1493T>C MANE Select	ENSP00000246914.4:p.Val498Ala
ENST00000246914.9:c.1493T>C	ENSP00000246914.4:p.Val498Ala
ENST00000587705.5:n.173T>C
ENST00000591448.5:c.1404T>C	ENSP00000467088.1:p.Gly468=
ENST00000592072.1:n.173T>C
NM_032387.4:c.1493T>C	NP_115763.2:p.Val498Ala
XM_005257595.3:c.1493T>C	XP_005257652.1:p.Val498Ala
XM_005257596.2:c.1493T>C	XP_005257653.1:p.Val498Ala
XM_005257597.3:c.1493T>C	XP_005257654.1:p.Val498Ala
XM_006722020.2:c.1493T>C	XP_006722083.1:p.Val498Ala
XM_006722021.1:c.485T>C	XP_006722084.1:p.Val162Ala
XM_006722022.1:c.485T>C	XP_006722085.1:p.Val162Ala
XM_011525132.1:c.1493T>C	XP_011523434.1:p.Val498Ala
XM_011525133.1:c.1493T>C	XP_011523435.1:p.Val498Ala
XM_011525134.1:c.1493T>C	XP_011523436.1:p.Val498Ala
XM_011525135.1:c.1493T>C	XP_011523437.1:p.Val498Ala
NM_001321299.1:c.485T>C	NP_001308228.1:p.Val162Ala
XM_017024962.1:c.1493T>C	XP_016880451.1:p.Val498Ala
XM_017024966.1:c.485T>C	XP_016880455.1:p.Val162Ala
NM_032387.5:c.1493T>C MANE Select	NP_115763.2:p.Val498Ala
NM_001321299.2:c.485T>C	NP_001308228.1:p.Val162Ala