Canonical Allele Identifier: CA1155658597
Gene: CLCNKB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16051726C= , CM000663.2:g.16051726C= GRCh38
NC_000001.10:g.16378221C= , CM000663.1:g.16378221C= GRCh37
NC_000001.9:g.16250808C= NCBI36
NG_013079.1:g.12975C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682338.1:c.1314C= ENSP00000507062.1:p.Arg438=
ENST00000682793.1:c.1314C= ENSP00000506910.1:p.Arg438=
ENST00000682838.1:c.*1056C= ENSP00000507652.1:n.*1056C=
ENST00000683578.1:c.1314C= ENSP00000507430.1:p.Arg438=
ENST00000683606.1:n.929C=
ENST00000683661.1:n.2849C=
ENST00000684324.1:c.1314C= ENSP00000507937.1:p.Arg438=
ENST00000684545.1:c.1314C= ENSP00000506733.1:p.Arg438=
ENST00000684624.1:n.691C=
ENST00000684714.1:c.1314C= ENSP00000506861.1:p.Arg438=
ENST00000684731.1:n.775C=
ENST00000375679.9:c.1314C= MANE Select ENSP00000364831.5:p.Arg438=
ENST00000375667.7:c.807C= ENSP00000364819.3:p.Arg269=
ENST00000375679.8:c.1314C= ENSP00000364831.4:p.Arg438=
ENST00000619181.4:c.933C= ENSP00000483866.1:p.Arg311=
NM_000085.4:c.1314C= NP_000076.2:p.Arg438=
NM_001165945.2:c.807C= NP_001159417.2:p.Arg269=
XM_011540619.1:c.1155C= XP_011538921.1:p.Arg385=
XM_011540620.1:c.1314C= XP_011538922.1:p.Arg438=
XM_011540621.1:c.663C= XP_011538923.1:p.Arg221=
NM_000085.5:c.1314C= MANE Select NP_000076.2:p.Arg438=