Canonical Allele Identifier: CA2643570379

Gene: CLCNKB

Linked Data

• gnomAD v4: 1-16052051-A-AGCCCAGGCACTGGGCACTTCCCACAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052060_16052086dup , CM000663.2:g.16052060_16052086dup	GRCh38
NC_000001.10:g.16378555_16378581dup , CM000663.1:g.16378555_16378581dup	GRCh37
NC_000001.9:g.16251142_16251168dup	NCBI36
NG_013079.1:g.13309_13335dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1409-138_1409-112dup	ENSP00000507062.1:n.1409-138_1409-112dup
ENST00000682793.1:c.1409-138_1409-112dup	ENSP00000506910.1:n.1409-138_1409-112dup
ENST00000682838.1:c.*1151-138_*1151-112dup	ENSP00000507652.1:n.*1151-138_*1151-112dup
ENST00000683578.1:c.1409-138_1409-112dup	ENSP00000507430.1:n.1409-138_1409-112dup
ENST00000683606.1:n.1024-147_1024-121dup
ENST00000683661.1:n.2944-138_2944-112dup
ENST00000684324.1:c.1409-138_1409-112dup	ENSP00000507937.1:n.1409-138_1409-112dup
ENST00000684545.1:c.1409-138_1409-112dup	ENSP00000506733.1:n.1409-138_1409-112dup
ENST00000684624.1:n.786-138_786-112dup
ENST00000684714.1:c.1409-138_1409-112dup	ENSP00000506861.1:n.1409-138_1409-112dup
ENST00000684731.1:n.870-138_870-112dup
ENST00000375679.9:c.1409-138_1409-112dup MANE Select	ENSP00000364831.5:n.1409-138_1409-112dup
ENST00000375667.7:c.902-138_902-112dup	ENSP00000364819.3:n.902-138_902-112dup
ENST00000375679.8:c.1409-138_1409-112dup	ENSP00000364831.4:n.1409-138_1409-112dup
ENST00000619181.4:c.1028-138_1028-112dup	ENSP00000483866.1:n.1028-138_1028-112dup
NM_000085.4:c.1409-138_1409-112dup	NP_000076.2:n.1409-138_1409-112dup
NM_001165945.2:c.902-138_902-112dup	NP_001159417.2:n.902-138_902-112dup
XM_011540619.1:c.1250-138_1250-112dup	XP_011538921.1:n.1250-138_1250-112dup
XM_011540620.1:c.1409-138_1409-112dup	XP_011538922.1:n.1409-138_1409-112dup
XM_011540621.1:c.758-138_758-112dup	XP_011538923.1:n.758-138_758-112dup
NM_000085.5:c.1409-138_1409-112dup MANE Select	NP_000076.2:n.1409-138_1409-112dup