Canonical Allele Identifier: CA2260641778

Gene: WNK4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787206_42787209delinsCAAG , CM000679.2:g.42787206_42787209delinsCAAG	GRCh38
NC_000017.10:g.40939224_40939227delinsCAAG , CM000679.1:g.40939224_40939227delinsCAAG	GRCh37
NC_000017.9:g.38192750_38192753delinsCAAG	NCBI36
NG_016227.1:g.11576_11579delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1477-72_1477-69delinsCAAG MANE Select	ENSP00000246914.4:n.1477-72_1477-69delinsCAAG
ENST00000246914.9:c.1477-72_1477-69delinsCAAG	ENSP00000246914.4:n.1477-72_1477-69delinsCAAG
ENST00000587705.5:n.157-72_157-69delinsCAAG
ENST00000591448.5:c.1388-72_1388-69delinsCAAG	ENSP00000467088.1:n.1388-72_1388-69delinsCAAG
ENST00000592072.1:n.157-72_157-69delinsCAAG
NM_032387.4:c.1477-72_1477-69delinsCAAG	NP_115763.2:n.1477-72_1477-69delinsCAAG
XM_005257595.3:c.1477-72_1477-69delinsCAAG	XP_005257652.1:n.1477-72_1477-69delinsCAAG
XM_005257596.2:c.1477-72_1477-69delinsCAAG	XP_005257653.1:n.1477-72_1477-69delinsCAAG
XM_005257597.3:c.1477-72_1477-69delinsCAAG	XP_005257654.1:n.1477-72_1477-69delinsCAAG
XM_006722020.2:c.1477-72_1477-69delinsCAAG	XP_006722083.1:n.1477-72_1477-69delinsCAAG
XM_006722021.1:c.469-72_469-69delinsCAAG	XP_006722084.1:n.469-72_469-69delinsCAAG
XM_006722022.1:c.469-72_469-69delinsCAAG	XP_006722085.1:n.469-72_469-69delinsCAAG
XM_011525132.1:c.1477-72_1477-69delinsCAAG	XP_011523434.1:n.1477-72_1477-69delinsCAAG
XM_011525133.1:c.1477-72_1477-69delinsCAAG	XP_011523435.1:n.1477-72_1477-69delinsCAAG
XM_011525134.1:c.1477-72_1477-69delinsCAAG	XP_011523436.1:n.1477-72_1477-69delinsCAAG
XM_011525135.1:c.1477-72_1477-69delinsCAAG	XP_011523437.1:n.1477-72_1477-69delinsCAAG
NM_001321299.1:c.469-72_469-69delinsCAAG	NP_001308228.1:n.469-72_469-69delinsCAAG
XM_017024962.1:c.1477-72_1477-69delinsCAAG	XP_016880451.1:n.1477-72_1477-69delinsCAAG
XM_017024966.1:c.469-72_469-69delinsCAAG	XP_016880455.1:n.469-72_469-69delinsCAAG
NM_032387.5:c.1477-72_1477-69delinsCAAG MANE Select	NP_115763.2:n.1477-72_1477-69delinsCAAG
NM_001321299.2:c.469-72_469-69delinsCAAG	NP_001308228.1:n.469-72_469-69delinsCAAG