Canonical Allele Identifier: CA1140620079

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052005_16052012delinsTCCTGTCC , CM000663.2:g.16052005_16052012delinsTCCTGTCC	GRCh38
NC_000001.10:g.16378500_16378507delinsTCCTGTCC , CM000663.1:g.16378500_16378507delinsTCCTGTCC	GRCh37
NC_000001.9:g.16251087_16251094delinsTCCTGTCC	NCBI36
NG_013079.1:g.13254_13261delinsTCCTGTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1408+185_1409-186delinsTCCTGTCC	ENSP00000507062.1:n.1408+185_1409-186delinsTCCTGTCC
ENST00000682793.1:c.1408+185_1409-186delinsTCCTGTCC	ENSP00000506910.1:n.1408+185_1409-186delinsTCCTGTCC
ENST00000682838.1:c.*1150+185_*1151-186delinsTCCTGTCC	ENSP00000507652.1:n.*1150+185_*1151-186delinsTCCTGTCC
ENST00000683578.1:c.1408+185_1409-186delinsTCCTGTCC	ENSP00000507430.1:n.1408+185_1409-186delinsTCCTGTCC
ENST00000683606.1:n.1023+185_1023+192delinsTCCTGTCC
ENST00000683661.1:n.2943+185_2944-186delinsTCCTGTCC
ENST00000684324.1:c.1408+185_1409-186delinsTCCTGTCC	ENSP00000507937.1:n.1408+185_1409-186delinsTCCTGTCC
ENST00000684545.1:c.1408+185_1409-186delinsTCCTGTCC	ENSP00000506733.1:n.1408+185_1409-186delinsTCCTGTCC
ENST00000684624.1:n.785+185_786-186delinsTCCTGTCC
ENST00000684714.1:c.1408+185_1409-186delinsTCCTGTCC	ENSP00000506861.1:n.1408+185_1409-186delinsTCCTGTCC
ENST00000684731.1:n.869+185_870-186delinsTCCTGTCC
ENST00000375679.9:c.1408+185_1409-186delinsTCCTGTCC MANE Select	ENSP00000364831.5:n.1408+185_1409-186delinsTCCTGTCC
ENST00000375667.7:c.901+185_902-186delinsTCCTGTCC	ENSP00000364819.3:n.901+185_902-186delinsTCCTGTCC
ENST00000375679.8:c.1408+185_1409-186delinsTCCTGTCC	ENSP00000364831.4:n.1408+185_1409-186delinsTCCTGTCC
ENST00000619181.4:c.1027+185_1028-186delinsTCCTGTCC	ENSP00000483866.1:n.1027+185_1028-186delinsTCCTGTCC
NM_000085.4:c.1408+185_1409-186delinsTCCTGTCC	NP_000076.2:n.1408+185_1409-186delinsTCCTGTCC
NM_001165945.2:c.901+185_902-186delinsTCCTGTCC	NP_001159417.2:n.901+185_902-186delinsTCCTGTCC
XM_011540619.1:c.1249+185_1250-186delinsTCCTGTCC	XP_011538921.1:n.1249+185_1250-186delinsTCCTGTCC
XM_011540620.1:c.1408+185_1409-186delinsTCCTGTCC	XP_011538922.1:n.1408+185_1409-186delinsTCCTGTCC
XM_011540621.1:c.757+185_758-186delinsTCCTGTCC	XP_011538923.1:n.757+185_758-186delinsTCCTGTCC
NM_000085.5:c.1408+185_1409-186delinsTCCTGTCC MANE Select	NP_000076.2:n.1408+185_1409-186delinsTCCTGTCC