Canonical Allele Identifier: CA1155654962

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048262_16048263delinsTG , CM000663.2:g.16048262_16048263delinsTG	GRCh38
NC_000001.10:g.16374757_16374758delinsTG , CM000663.1:g.16374757_16374758delinsTG	GRCh37
NC_000001.9:g.16247344_16247345delinsTG	NCBI36
NG_013079.1:g.9511_9512delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.499-81_499-80delinsTG	ENSP00000507062.1:n.499-81_499-80delinsTG
ENST00000682793.1:c.499-81_499-80delinsTG	ENSP00000506910.1:n.499-81_499-80delinsTG
ENST00000682838.1:c.*157-81_*157-80delinsTG	ENSP00000507652.1:n.*157-81_*157-80delinsTG
ENST00000683578.1:c.499-81_499-80delinsTG	ENSP00000507430.1:n.499-81_499-80delinsTG
ENST00000683661.1:n.2034-81_2034-80delinsTG
ENST00000684324.1:c.499-81_499-80delinsTG	ENSP00000507937.1:n.499-81_499-80delinsTG
ENST00000684545.1:c.499-81_499-80delinsTG	ENSP00000506733.1:n.499-81_499-80delinsTG
ENST00000684714.1:c.499-81_499-80delinsTG	ENSP00000506861.1:n.499-81_499-80delinsTG
ENST00000375679.9:c.499-81_499-80delinsTG MANE Select	ENSP00000364831.5:n.499-81_499-80delinsTG
ENST00000375679.8:c.499-81_499-80delinsTG	ENSP00000364831.4:n.499-81_499-80delinsTG
ENST00000619181.4:c.499-81_499-80delinsTG	ENSP00000483866.1:n.499-81_499-80delinsTG
NM_000085.4:c.499-81_499-80delinsTG	NP_000076.2:n.499-81_499-80delinsTG
XM_011540619.1:c.340-81_340-80delinsTG	XP_011538921.1:n.340-81_340-80delinsTG
XM_011540620.1:c.499-81_499-80delinsTG	XP_011538922.1:n.499-81_499-80delinsTG
NM_000085.5:c.499-81_499-80delinsTG MANE Select	NP_000076.2:n.499-81_499-80delinsTG