Canonical Allele Identifier: CA2643565240
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16055549_16055559del , CM000663.2:g.16055549_16055559del GRCh38
NC_000001.10:g.16382044_16382054del , CM000663.1:g.16382044_16382054del GRCh37
NC_000001.9:g.16254631_16254641del NCBI36
NG_013079.1:g.16798_16808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1845+26_1845+36del ENSP00000507062.1:n.1845+26_1845+36del
ENST00000682793.1:c.1845+26_1845+36del ENSP00000506910.1:n.1845+26_1845+36del
ENST00000682838.1:c.*1587+26_*1587+36del ENSP00000507652.1:n.*1587+26_*1587+36del
ENST00000683578.1:c.1845+26_1845+36del ENSP00000507430.1:n.1845+26_1845+36del
ENST00000683606.1:n.1451+26_1451+36del
ENST00000683661.1:n.3380+26_3380+36del
ENST00000684324.1:c.1845+26_1845+36del ENSP00000507937.1:n.1845+26_1845+36del
ENST00000684545.1:c.1845+26_1845+36del ENSP00000506733.1:n.1845+26_1845+36del
ENST00000684624.1:n.1222+26_1222+36del
ENST00000684714.1:c.*65+26_*65+36del ENSP00000506861.1:n.*65+26_*65+36del
ENST00000684731.1:n.1172+26_1172+36del
ENST00000375679.9:c.1845+26_1845+36del MANE Select ENSP00000364831.5:n.1845+26_1845+36del
ENST00000375667.7:c.1338+26_1338+36del ENSP00000364819.3:n.1338+26_1338+36del
ENST00000375679.8:c.1845+26_1845+36del ENSP00000364831.4:n.1845+26_1845+36del
ENST00000431772.1:c.312+26_312+36del ENSP00000389344.1:n.312+26_312+36del
ENST00000619181.4:c.1294-1638_1294-1628del ENSP00000483866.1:n.1294-1638_1294-1628del
NM_000085.4:c.1845+26_1845+36del NP_000076.2:n.1845+26_1845+36del
NM_001165945.2:c.1338+26_1338+36del NP_001159417.2:n.1338+26_1338+36del
XM_011540619.1:c.1686+26_1686+36del XP_011538921.1:n.1686+26_1686+36del
XM_011540621.1:c.1194+26_1194+36del XP_011538923.1:n.1194+26_1194+36del
NM_000085.5:c.1845+26_1845+36del MANE Select NP_000076.2:n.1845+26_1845+36del