Canonical Allele Identifier: CA1155658742

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052062_16052063delinsTG , CM000663.2:g.16052062_16052063delinsTG	GRCh38
NC_000001.10:g.16378557_16378558delinsTG , CM000663.1:g.16378557_16378558delinsTG	GRCh37
NC_000001.9:g.16251144_16251145delinsTG	NCBI36
NG_013079.1:g.13311_13312delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1409-136_1409-135delinsTG	ENSP00000507062.1:n.1409-136_1409-135delinsTG
ENST00000682793.1:c.1409-136_1409-135delinsTG	ENSP00000506910.1:n.1409-136_1409-135delinsTG
ENST00000682838.1:c.*1151-136_*1151-135delinsTG	ENSP00000507652.1:n.*1151-136_*1151-135delinsTG
ENST00000683578.1:c.1409-136_1409-135delinsTG	ENSP00000507430.1:n.1409-136_1409-135delinsTG
ENST00000683606.1:n.1024-145_1024-144delinsTG
ENST00000683661.1:n.2944-136_2944-135delinsTG
ENST00000684324.1:c.1409-136_1409-135delinsTG	ENSP00000507937.1:n.1409-136_1409-135delinsTG
ENST00000684545.1:c.1409-136_1409-135delinsTG	ENSP00000506733.1:n.1409-136_1409-135delinsTG
ENST00000684624.1:n.786-136_786-135delinsTG
ENST00000684714.1:c.1409-136_1409-135delinsTG	ENSP00000506861.1:n.1409-136_1409-135delinsTG
ENST00000684731.1:n.870-136_870-135delinsTG
ENST00000375679.9:c.1409-136_1409-135delinsTG MANE Select	ENSP00000364831.5:n.1409-136_1409-135delinsTG
ENST00000375667.7:c.902-136_902-135delinsTG	ENSP00000364819.3:n.902-136_902-135delinsTG
ENST00000375679.8:c.1409-136_1409-135delinsTG	ENSP00000364831.4:n.1409-136_1409-135delinsTG
ENST00000619181.4:c.1028-136_1028-135delinsTG	ENSP00000483866.1:n.1028-136_1028-135delinsTG
NM_000085.4:c.1409-136_1409-135delinsTG	NP_000076.2:n.1409-136_1409-135delinsTG
NM_001165945.2:c.902-136_902-135delinsTG	NP_001159417.2:n.902-136_902-135delinsTG
XM_011540619.1:c.1250-136_1250-135delinsTG	XP_011538921.1:n.1250-136_1250-135delinsTG
XM_011540620.1:c.1409-136_1409-135delinsTG	XP_011538922.1:n.1409-136_1409-135delinsTG
XM_011540621.1:c.758-136_758-135delinsTG	XP_011538923.1:n.758-136_758-135delinsTG
NM_000085.5:c.1409-136_1409-135delinsTG MANE Select	NP_000076.2:n.1409-136_1409-135delinsTG