Canonical Allele Identifier: CA1155658715
Gene: CLCNKB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16052004C= , CM000663.2:g.16052004C= GRCh38
NC_000001.10:g.16378499C= , CM000663.1:g.16378499C= GRCh37
NC_000001.9:g.16251086C= NCBI36
NG_013079.1:g.13253C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1408+184C= ENSP00000507062.1:n.1408+184C=
ENST00000682793.1:c.1408+184C= ENSP00000506910.1:n.1408+184C=
ENST00000682838.1:c.*1150+184C= ENSP00000507652.1:n.*1150+184C=
ENST00000683578.1:c.1408+184C= ENSP00000507430.1:n.1408+184C=
ENST00000683606.1:n.1023+184C=
ENST00000683661.1:n.2943+184C=
ENST00000684324.1:c.1408+184C= ENSP00000507937.1:n.1408+184C=
ENST00000684545.1:c.1408+184C= ENSP00000506733.1:n.1408+184C=
ENST00000684624.1:n.785+184C=
ENST00000684714.1:c.1408+184C= ENSP00000506861.1:n.1408+184C=
ENST00000684731.1:n.869+184C=
ENST00000375679.9:c.1408+184C= MANE Select ENSP00000364831.5:n.1408+184C=
ENST00000375667.7:c.901+184C= ENSP00000364819.3:n.901+184C=
ENST00000375679.8:c.1408+184C= ENSP00000364831.4:n.1408+184C=
ENST00000619181.4:c.1027+184C= ENSP00000483866.1:n.1027+184C=
NM_000085.4:c.1408+184C= NP_000076.2:n.1408+184C=
NM_001165945.2:c.901+184C= NP_001159417.2:n.901+184C=
XM_011540619.1:c.1249+184C= XP_011538921.1:n.1249+184C=
XM_011540620.1:c.1408+184C= XP_011538922.1:n.1408+184C=
XM_011540621.1:c.757+184C= XP_011538923.1:n.757+184C=
NM_000085.5:c.1408+184C= MANE Select NP_000076.2:n.1408+184C=