Canonical Allele Identifier: CA1155658716

Gene: CLCNKB

Linked Data

• dbSNP Id: rs2023310218

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052004_16052005insACCTG , CM000663.2:g.16052004_16052005insACCTG	GRCh38
NC_000001.10:g.16378499_16378500insACCTG , CM000663.1:g.16378499_16378500insACCTG	GRCh37
NC_000001.9:g.16251086_16251087insACCTG	NCBI36
NG_013079.1:g.13253_13254insACCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1408+184_1408+185insACCTG	ENSP00000507062.1:n.1408+184_1408+185insACCTG
ENST00000682793.1:c.1408+184_1408+185insACCTG	ENSP00000506910.1:n.1408+184_1408+185insACCTG
ENST00000682838.1:c.*1150+184_*1150+185insACCTG	ENSP00000507652.1:n.*1150+184_*1150+185insACCTG
ENST00000683578.1:c.1408+184_1408+185insACCTG	ENSP00000507430.1:n.1408+184_1408+185insACCTG
ENST00000683606.1:n.1023+184_1023+185insACCTG
ENST00000683661.1:n.2943+184_2943+185insACCTG
ENST00000684324.1:c.1408+184_1408+185insACCTG	ENSP00000507937.1:n.1408+184_1408+185insACCTG
ENST00000684545.1:c.1408+184_1408+185insACCTG	ENSP00000506733.1:n.1408+184_1408+185insACCTG
ENST00000684624.1:n.785+184_785+185insACCTG
ENST00000684714.1:c.1408+184_1408+185insACCTG	ENSP00000506861.1:n.1408+184_1408+185insACCTG
ENST00000684731.1:n.869+184_869+185insACCTG
ENST00000375679.9:c.1408+184_1408+185insACCTG MANE Select	ENSP00000364831.5:n.1408+184_1408+185insACCTG
ENST00000375667.7:c.901+184_901+185insACCTG	ENSP00000364819.3:n.901+184_901+185insACCTG
ENST00000375679.8:c.1408+184_1408+185insACCTG	ENSP00000364831.4:n.1408+184_1408+185insACCTG
ENST00000619181.4:c.1027+184_1027+185insACCTG	ENSP00000483866.1:n.1027+184_1027+185insACCTG
NM_000085.4:c.1408+184_1408+185insACCTG	NP_000076.2:n.1408+184_1408+185insACCTG
NM_001165945.2:c.901+184_901+185insACCTG	NP_001159417.2:n.901+184_901+185insACCTG
XM_011540619.1:c.1249+184_1249+185insACCTG	XP_011538921.1:n.1249+184_1249+185insACCTG
XM_011540620.1:c.1408+184_1408+185insACCTG	XP_011538922.1:n.1408+184_1408+185insACCTG
XM_011540621.1:c.757+184_757+185insACCTG	XP_011538923.1:n.757+184_757+185insACCTG
NM_000085.5:c.1408+184_1408+185insACCTG MANE Select	NP_000076.2:n.1408+184_1408+185insACCTG