Canonical Allele Identifier: CA500225353

Gene: WNK4

Linked Data

• MyVariant Identifiers: chr17:g.40939307C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787289C>G , CM000679.2:g.42787289C>G	GRCh38
NC_000017.10:g.40939307C>G , CM000679.1:g.40939307C>G	GRCh37
NC_000017.9:g.38192833C>G	NCBI36
NG_016227.1:g.11659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1488C>G MANE Select	ENSP00000246914.4:p.Gly496=
ENST00000246914.9:c.1488C>G	ENSP00000246914.4:p.Gly496=
ENST00000587705.5:n.168C>G
ENST00000591448.5:c.1399C>G	ENSP00000467088.1:p.Leu467Val
ENST00000592072.1:n.168C>G
NM_032387.4:c.1488C>G	NP_115763.2:p.Gly496=
XM_005257595.3:c.1488C>G	XP_005257652.1:p.Gly496=
XM_005257596.2:c.1488C>G	XP_005257653.1:p.Gly496=
XM_005257597.3:c.1488C>G	XP_005257654.1:p.Gly496=
XM_006722020.2:c.1488C>G	XP_006722083.1:p.Gly496=
XM_006722021.1:c.480C>G	XP_006722084.1:p.Gly160=
XM_006722022.1:c.480C>G	XP_006722085.1:p.Gly160=
XM_011525132.1:c.1488C>G	XP_011523434.1:p.Gly496=
XM_011525133.1:c.1488C>G	XP_011523435.1:p.Gly496=
XM_011525134.1:c.1488C>G	XP_011523436.1:p.Gly496=
XM_011525135.1:c.1488C>G	XP_011523437.1:p.Gly496=
NM_001321299.1:c.480C>G	NP_001308228.1:p.Gly160=
XM_017024962.1:c.1488C>G	XP_016880451.1:p.Gly496=
XM_017024966.1:c.480C>G	XP_016880455.1:p.Gly160=
NM_032387.5:c.1488C>G MANE Select	NP_115763.2:p.Gly496=
NM_001321299.2:c.480C>G	NP_001308228.1:p.Gly160=