Canonical Allele Identifier: CA645572785

Gene: WNK4

Linked Data

• COSMIC: COSM272114 ; COSM272115

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42787432_42787433del , CM000679.2:g.42787432_42787433del	GRCh38
NC_000017.10:g.40939450_40939451del , CM000679.1:g.40939450_40939451del	GRCh37
NC_000017.9:g.38192976_38192977del	NCBI36
NG_016227.1:g.11802_11803del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246914.10:c.1631_1632del MANE Select	ENSP00000246914.4:p.Val544AlafsTer13
ENST00000246914.9:c.1631_1632del	ENSP00000246914.4:p.Val544AlafsTer13
ENST00000587705.5:n.311_312del
ENST00000591448.5:c.*132_*133del	ENSP00000467088.1:n.*132_*133del
ENST00000592072.1:n.311_312del
NM_032387.4:c.1631_1632del	NP_115763.2:p.Val544AlafsTer13
XM_005257595.3:c.1631_1632del	XP_005257652.1:p.Val544AlafsTer13
XM_005257596.2:c.1631_1632del	XP_005257653.1:p.Val544AlafsTer13
XM_005257597.3:c.1631_1632del	XP_005257654.1:p.Val544AlafsTer13
XM_006722020.2:c.1631_1632del	XP_006722083.1:p.Val544AlafsTer13
XM_006722021.1:c.623_624del	XP_006722084.1:p.Val208AlafsTer13
XM_006722022.1:c.623_624del	XP_006722085.1:p.Val208AlafsTer13
XM_011525132.1:c.1631_1632del	XP_011523434.1:p.Val544AlafsTer13
XM_011525133.1:c.1631_1632del	XP_011523435.1:p.Val544AlafsTer13
XM_011525134.1:c.1631_1632del	XP_011523436.1:p.Val544AlafsTer13
XM_011525135.1:c.1631_1632del	XP_011523437.1:p.Val544AlafsTer13
NM_001321299.1:c.623_624del	NP_001308228.1:p.Val208AlafsTer13
XM_017024962.1:c.1631_1632del	XP_016880451.1:p.Val544AlafsTer13
XM_017024966.1:c.623_624del	XP_016880455.1:p.Val208AlafsTer13
NM_032387.5:c.1631_1632del MANE Select	NP_115763.2:p.Val544AlafsTer13
NM_001321299.2:c.623_624del	NP_001308228.1:p.Val208AlafsTer13