Canonical Allele Identifier: CA2643565507
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16055564_16055565insGGTGGGGGTGGGGGGGGGGGTGGG , CM000663.2:g.16055564_16055565insGGTGGGGGTGGGGGGGGGGGTGGG GRCh38
NC_000001.10:g.16382059_16382060insGGTGGGGGTGGGGGGGGGGGTGGG , CM000663.1:g.16382059_16382060insGGTGGGGGTGGGGGGGGGGGTGGG GRCh37
NC_000001.9:g.16254646_16254647insGGTGGGGGTGGGGGGGGGGGTGGG NCBI36
NG_013079.1:g.16813_16814insGGTGGGGGTGGGGGGGGGGGTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000507062.1:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000682793.1:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000506910.1:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000682838.1:c.*1587+41_*1587+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000507652.1:n.*1587+41_*1587+42insGGTGGGGGTGGGGGGGGGGGT...
ENST00000683578.1:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000507430.1:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000683606.1:n.1451+41_1451+42insGGTGGGGGTGGGGGGGGGGGTGGG
ENST00000683661.1:n.3380+41_3380+42insGGTGGGGGTGGGGGGGGGGGTGGG
ENST00000684324.1:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000507937.1:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000684545.1:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000506733.1:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000684624.1:n.1222+41_1222+42insGGTGGGGGTGGGGGGGGGGGTGGG
ENST00000684714.1:c.*65+41_*65+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000506861.1:n.*65+41_*65+42insGGTGGGGGTGGGGGGGGGGGTGGG
ENST00000684731.1:n.1172+41_1172+42insGGTGGGGGTGGGGGGGGGGGTGGG
ENST00000375679.9:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG MANE Select ENSP00000364831.5:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000375667.7:c.1338+41_1338+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000364819.3:n.1338+41_1338+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000375679.8:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000364831.4:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGG...
ENST00000431772.1:c.312+41_312+42insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000389344.1:n.312+41_312+42insGGTGGGGGTGGGGGGGGGGGTGGG
ENST00000619181.4:c.1294-1623_1294-1622insGGTGGGGGTGGGGGGGGGGGTGGG ENSP00000483866.1:n.1294-1623_1294-1622insGGTGGGGGTGGGGGGGGGG...
NM_000085.4:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG NP_000076.2:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG
NM_001165945.2:c.1338+41_1338+42insGGTGGGGGTGGGGGGGGGGGTGGG NP_001159417.2:n.1338+41_1338+42insGGTGGGGGTGGGGGGGGGGGTGGG
XM_011540619.1:c.1686+41_1686+42insGGTGGGGGTGGGGGGGGGGGTGGG XP_011538921.1:n.1686+41_1686+42insGGTGGGGGTGGGGGGGGGGGTGGG
XM_011540621.1:c.1194+41_1194+42insGGTGGGGGTGGGGGGGGGGGTGGG XP_011538923.1:n.1194+41_1194+42insGGTGGGGGTGGGGGGGGGGGTGGG
NM_000085.5:c.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG MANE Select NP_000076.2:n.1845+41_1845+42insGGTGGGGGTGGGGGGGGGGGTGGG