Canonical Allele Identifier: CA1155658718

Gene: CLCNKB

Linked Data

• dbSNP Id: rs2023310548

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052010_16052011insTCTGT , CM000663.2:g.16052010_16052011insTCTGT	GRCh38
NC_000001.10:g.16378505_16378506insTCTGT , CM000663.1:g.16378505_16378506insTCTGT	GRCh37
NC_000001.9:g.16251092_16251093insTCTGT	NCBI36
NG_013079.1:g.13259_13260insTCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1409-188_1409-187insTCTGT	ENSP00000507062.1:n.1409-188_1409-187insTCTGT
ENST00000682793.1:c.1409-188_1409-187insTCTGT	ENSP00000506910.1:n.1409-188_1409-187insTCTGT
ENST00000682838.1:c.*1151-188_*1151-187insTCTGT	ENSP00000507652.1:n.*1151-188_*1151-187insTCTGT
ENST00000683578.1:c.1409-188_1409-187insTCTGT	ENSP00000507430.1:n.1409-188_1409-187insTCTGT
ENST00000683606.1:n.1023+190_1023+191insTCTGT
ENST00000683661.1:n.2944-188_2944-187insTCTGT
ENST00000684324.1:c.1409-188_1409-187insTCTGT	ENSP00000507937.1:n.1409-188_1409-187insTCTGT
ENST00000684545.1:c.1409-188_1409-187insTCTGT	ENSP00000506733.1:n.1409-188_1409-187insTCTGT
ENST00000684624.1:n.786-188_786-187insTCTGT
ENST00000684714.1:c.1409-188_1409-187insTCTGT	ENSP00000506861.1:n.1409-188_1409-187insTCTGT
ENST00000684731.1:n.870-188_870-187insTCTGT
ENST00000375679.9:c.1409-188_1409-187insTCTGT MANE Select	ENSP00000364831.5:n.1409-188_1409-187insTCTGT
ENST00000375667.7:c.902-188_902-187insTCTGT	ENSP00000364819.3:n.902-188_902-187insTCTGT
ENST00000375679.8:c.1409-188_1409-187insTCTGT	ENSP00000364831.4:n.1409-188_1409-187insTCTGT
ENST00000619181.4:c.1028-188_1028-187insTCTGT	ENSP00000483866.1:n.1028-188_1028-187insTCTGT
NM_000085.4:c.1409-188_1409-187insTCTGT	NP_000076.2:n.1409-188_1409-187insTCTGT
NM_001165945.2:c.902-188_902-187insTCTGT	NP_001159417.2:n.902-188_902-187insTCTGT
XM_011540619.1:c.1250-188_1250-187insTCTGT	XP_011538921.1:n.1250-188_1250-187insTCTGT
XM_011540620.1:c.1409-188_1409-187insTCTGT	XP_011538922.1:n.1409-188_1409-187insTCTGT
XM_011540621.1:c.758-188_758-187insTCTGT	XP_011538923.1:n.758-188_758-187insTCTGT
NM_000085.5:c.1409-188_1409-187insTCTGT MANE Select	NP_000076.2:n.1409-188_1409-187insTCTGT