Canonical Allele Identifier: CA2643569547
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16051639_16051640insCGTCCTCAGTACAACCTGGGGAC , CM000663.2:g.16051639_16051640insCGTCCTCAGTACAACCTGGGGAC GRCh38
NC_000001.10:g.16378134_16378135insCGTCCTCAGTACAACCTGGGGAC , CM000663.1:g.16378134_16378135insCGTCCTCAGTACAACCTGGGGAC GRCh37
NC_000001.9:g.16250721_16250722insCGTCCTCAGTACAACCTGGGGAC NCBI36
NG_013079.1:g.12888_12889insCGTCCTCAGTACAACCTGGGGAC

Transcript Alleles

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