Canonical Allele Identifier: CA2733784814

Gene: WNK4

Linked Data

• dbSNP Id: rs2144033817

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787437_42787438insGGGGGGGGGGGGGGGGGGG , CM000679.2:g.42787437_42787438insGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000017.10:g.40939455_40939456insGGGGGGGGGGGGGGGGGGG , CM000679.1:g.40939455_40939456insGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000017.9:g.38192981_38192982insGGGGGGGGGGGGGGGGGGG	NCBI36
NG_016227.1:g.11807_11808insGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1636_1637insGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000246914.4:p.Met546ArgfsTer18
ENST00000246914.9:c.1636_1637insGGGGGGGGGGGGGGGGGGG	ENSP00000246914.4:p.Met546ArgfsTer18
ENST00000587705.5:n.316_317insGGGGGGGGGGGGGGGGGGG
ENST00000591448.5:c.*137_*138insGGGGGGGGGGGGGGGGGGG	ENSP00000467088.1:n.*137_*138insGGGGGGGGGGGGGGGGGGG
ENST00000592072.1:n.316_317insGGGGGGGGGGGGGGGGGGG
NM_032387.4:c.1636_1637insGGGGGGGGGGGGGGGGGGG	NP_115763.2:p.Met546ArgfsTer18
XM_005257595.3:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_005257652.1:p.Met546ArgfsTer18
XM_005257596.2:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_005257653.1:p.Met546ArgfsTer18
XM_005257597.3:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_005257654.1:p.Met546ArgfsTer18
XM_006722020.2:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_006722083.1:p.Met546ArgfsTer18
XM_006722021.1:c.628_629insGGGGGGGGGGGGGGGGGGG	XP_006722084.1:p.Met210ArgfsTer18
XM_006722022.1:c.628_629insGGGGGGGGGGGGGGGGGGG	XP_006722085.1:p.Met210ArgfsTer18
XM_011525132.1:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_011523434.1:p.Met546ArgfsTer18
XM_011525133.1:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_011523435.1:p.Met546ArgfsTer18
XM_011525134.1:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_011523436.1:p.Met546ArgfsTer18
XM_011525135.1:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_011523437.1:p.Met546ArgfsTer18
NM_001321299.1:c.628_629insGGGGGGGGGGGGGGGGGGG	NP_001308228.1:p.Met210ArgfsTer18
XM_017024962.1:c.1636_1637insGGGGGGGGGGGGGGGGGGG	XP_016880451.1:p.Met546ArgfsTer18
XM_017024966.1:c.628_629insGGGGGGGGGGGGGGGGGGG	XP_016880455.1:p.Met210ArgfsTer18
NM_032387.5:c.1636_1637insGGGGGGGGGGGGGGGGGGG MANE Select	NP_115763.2:p.Met546ArgfsTer18
NM_001321299.2:c.628_629insGGGGGGGGGGGGGGGGGGG	NP_001308228.1:p.Met210ArgfsTer18