Canonical Allele Identifier: CA8583996

Gene: WNK4

Linked Data

• dbSNP Id: rs200716779
• ExAC: 17:40939251 T / C
• gnomAD v2: 17-40939251-T-C
• gnomAD v3: 17-42787233-T-C
• gnomAD v4: 17-42787233-T-C
• MyVariant Identifiers: chr17:g.40939251T>C (hg19) ; chr17:g.42787233T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787233T>C , CM000679.2:g.42787233T>C	GRCh38
NC_000017.10:g.40939251T>C , CM000679.1:g.40939251T>C	GRCh37
NC_000017.9:g.38192777T>C	NCBI36
NG_016227.1:g.11603T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1477-45T>C MANE Select	ENSP00000246914.4:n.1477-45T>C
ENST00000246914.9:c.1477-45T>C	ENSP00000246914.4:n.1477-45T>C
ENST00000587705.5:n.157-45T>C
ENST00000591448.5:c.1388-45T>C	ENSP00000467088.1:n.1388-45T>C
ENST00000592072.1:n.157-45T>C
NM_032387.4:c.1477-45T>C	NP_115763.2:n.1477-45T>C
XM_005257595.3:c.1477-45T>C	XP_005257652.1:n.1477-45T>C
XM_005257596.2:c.1477-45T>C	XP_005257653.1:n.1477-45T>C
XM_005257597.3:c.1477-45T>C	XP_005257654.1:n.1477-45T>C
XM_006722020.2:c.1477-45T>C	XP_006722083.1:n.1477-45T>C
XM_006722021.1:c.469-45T>C	XP_006722084.1:n.469-45T>C
XM_006722022.1:c.469-45T>C	XP_006722085.1:n.469-45T>C
XM_011525132.1:c.1477-45T>C	XP_011523434.1:n.1477-45T>C
XM_011525133.1:c.1477-45T>C	XP_011523435.1:n.1477-45T>C
XM_011525134.1:c.1477-45T>C	XP_011523436.1:n.1477-45T>C
XM_011525135.1:c.1477-45T>C	XP_011523437.1:n.1477-45T>C
NM_001321299.1:c.469-45T>C	NP_001308228.1:n.469-45T>C
XM_017024962.1:c.1477-45T>C	XP_016880451.1:n.1477-45T>C
XM_017024966.1:c.469-45T>C	XP_016880455.1:n.469-45T>C
NM_032387.5:c.1477-45T>C MANE Select	NP_115763.2:n.1477-45T>C
NM_001321299.2:c.469-45T>C	NP_001308228.1:n.469-45T>C