Canonical Allele Identifier: CA2576279465
Gene: WNK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42787213_42787215dup , CM000679.2:g.42787213_42787215dup GRCh38
NC_000017.10:g.40939231_40939233dup , CM000679.1:g.40939231_40939233dup GRCh37
NC_000017.9:g.38192757_38192759dup NCBI36
NG_016227.1:g.11583_11585dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246914.10:c.1477-65_1477-63dup MANE Select ENSP00000246914.4:n.1477-65_1477-63dup
ENST00000246914.9:c.1477-65_1477-63dup ENSP00000246914.4:n.1477-65_1477-63dup
ENST00000587705.5:n.157-65_157-63dup
ENST00000591448.5:c.1388-65_1388-63dup ENSP00000467088.1:n.1388-65_1388-63dup
ENST00000592072.1:n.157-65_157-63dup
NM_032387.4:c.1477-65_1477-63dup NP_115763.2:n.1477-65_1477-63dup
XM_005257595.3:c.1477-65_1477-63dup XP_005257652.1:n.1477-65_1477-63dup
XM_005257596.2:c.1477-65_1477-63dup XP_005257653.1:n.1477-65_1477-63dup
XM_005257597.3:c.1477-65_1477-63dup XP_005257654.1:n.1477-65_1477-63dup
XM_006722020.2:c.1477-65_1477-63dup XP_006722083.1:n.1477-65_1477-63dup
XM_006722021.1:c.469-65_469-63dup XP_006722084.1:n.469-65_469-63dup
XM_006722022.1:c.469-65_469-63dup XP_006722085.1:n.469-65_469-63dup
XM_011525132.1:c.1477-65_1477-63dup XP_011523434.1:n.1477-65_1477-63dup
XM_011525133.1:c.1477-65_1477-63dup XP_011523435.1:n.1477-65_1477-63dup
XM_011525134.1:c.1477-65_1477-63dup XP_011523436.1:n.1477-65_1477-63dup
XM_011525135.1:c.1477-65_1477-63dup XP_011523437.1:n.1477-65_1477-63dup
NM_001321299.1:c.469-65_469-63dup NP_001308228.1:n.469-65_469-63dup
XM_017024962.1:c.1477-65_1477-63dup XP_016880451.1:n.1477-65_1477-63dup
XM_017024966.1:c.469-65_469-63dup XP_016880455.1:n.469-65_469-63dup
NM_032387.5:c.1477-65_1477-63dup MANE Select NP_115763.2:n.1477-65_1477-63dup
NM_001321299.2:c.469-65_469-63dup NP_001308228.1:n.469-65_469-63dup