Canonical Allele Identifier: CA1155658727

Gene: CLCNKB

Linked Data

• dbSNP Id: rs2023310954

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052027_16052029del , CM000663.2:g.16052027_16052029del	GRCh38
NC_000001.10:g.16378522_16378524del , CM000663.1:g.16378522_16378524del	GRCh37
NC_000001.9:g.16251109_16251111del	NCBI36
NG_013079.1:g.13276_13278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1409-171_1409-169del	ENSP00000507062.1:n.1409-171_1409-169del
ENST00000682793.1:c.1409-171_1409-169del	ENSP00000506910.1:n.1409-171_1409-169del
ENST00000682838.1:c.*1151-171_*1151-169del	ENSP00000507652.1:n.*1151-171_*1151-169del
ENST00000683578.1:c.1409-171_1409-169del	ENSP00000507430.1:n.1409-171_1409-169del
ENST00000683606.1:n.1024-180_1024-178del
ENST00000683661.1:n.2944-171_2944-169del
ENST00000684324.1:c.1409-171_1409-169del	ENSP00000507937.1:n.1409-171_1409-169del
ENST00000684545.1:c.1409-171_1409-169del	ENSP00000506733.1:n.1409-171_1409-169del
ENST00000684624.1:n.786-171_786-169del
ENST00000684714.1:c.1409-171_1409-169del	ENSP00000506861.1:n.1409-171_1409-169del
ENST00000684731.1:n.870-171_870-169del
ENST00000375679.9:c.1409-171_1409-169del MANE Select	ENSP00000364831.5:n.1409-171_1409-169del
ENST00000375667.7:c.902-171_902-169del	ENSP00000364819.3:n.902-171_902-169del
ENST00000375679.8:c.1409-171_1409-169del	ENSP00000364831.4:n.1409-171_1409-169del
ENST00000619181.4:c.1028-171_1028-169del	ENSP00000483866.1:n.1028-171_1028-169del
NM_000085.4:c.1409-171_1409-169del	NP_000076.2:n.1409-171_1409-169del
NM_001165945.2:c.902-171_902-169del	NP_001159417.2:n.902-171_902-169del
XM_011540619.1:c.1250-171_1250-169del	XP_011538921.1:n.1250-171_1250-169del
XM_011540620.1:c.1409-171_1409-169del	XP_011538922.1:n.1409-171_1409-169del
XM_011540621.1:c.758-171_758-169del	XP_011538923.1:n.758-171_758-169del
NM_000085.5:c.1409-171_1409-169del MANE Select	NP_000076.2:n.1409-171_1409-169del