Canonical Allele Identifier: CA2643569559
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16051639_16051640insCGTCCTCAGTACAACCTGGGGAG , CM000663.2:g.16051639_16051640insCGTCCTCAGTACAACCTGGGGAG GRCh38
NC_000001.10:g.16378134_16378135insCGTCCTCAGTACAACCTGGGGAG , CM000663.1:g.16378134_16378135insCGTCCTCAGTACAACCTGGGGAG GRCh37
NC_000001.9:g.16250721_16250722insCGTCCTCAGTACAACCTGGGGAG NCBI36
NG_013079.1:g.12888_12889insCGTCCTCAGTACAACCTGGGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000507062.1:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000682793.1:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000506910.1:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000682838.1:c.*1040-71_*1040-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000507652.1:n.*1040-71_*1040-70insCGTCCTCAGTACAACCTGGGG...
ENST00000683578.1:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000507430.1:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000683606.1:n.913-71_913-70insCGTCCTCAGTACAACCTGGGGAG
ENST00000683661.1:n.2833-71_2833-70insCGTCCTCAGTACAACCTGGGGAG
ENST00000684324.1:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000507937.1:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000684545.1:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000506733.1:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000684624.1:n.675-71_675-70insCGTCCTCAGTACAACCTGGGGAG
ENST00000684714.1:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000506861.1:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000684731.1:n.759-71_759-70insCGTCCTCAGTACAACCTGGGGAG
ENST00000375679.9:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG MANE Select ENSP00000364831.5:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000375667.7:c.791-71_791-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000364819.3:n.791-71_791-70insCGTCCTCAGTACAACCTGGGGAG
ENST00000375679.8:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000364831.4:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG...
ENST00000619181.4:c.917-71_917-70insCGTCCTCAGTACAACCTGGGGAG ENSP00000483866.1:n.917-71_917-70insCGTCCTCAGTACAACCTGGGGAG
NM_000085.4:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG NP_000076.2:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG
NM_001165945.2:c.791-71_791-70insCGTCCTCAGTACAACCTGGGGAG NP_001159417.2:n.791-71_791-70insCGTCCTCAGTACAACCTGGGGAG
XM_011540619.1:c.1139-71_1139-70insCGTCCTCAGTACAACCTGGGGAG XP_011538921.1:n.1139-71_1139-70insCGTCCTCAGTACAACCTGGGGAG
XM_011540620.1:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG XP_011538922.1:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG
XM_011540621.1:c.647-71_647-70insCGTCCTCAGTACAACCTGGGGAG XP_011538923.1:n.647-71_647-70insCGTCCTCAGTACAACCTGGGGAG
NM_000085.5:c.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG MANE Select NP_000076.2:n.1298-71_1298-70insCGTCCTCAGTACAACCTGGGGAG