Canonical Allele Identifier: CA1155658601

Gene: CLCNKB

Linked Data

• dbSNP Id: rs2023301324

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051736dup , CM000663.2:g.16051736dup	GRCh38
NC_000001.10:g.16378231dup , CM000663.1:g.16378231dup	GRCh37
NC_000001.9:g.16250818dup	NCBI36
NG_013079.1:g.12985dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1324dup	ENSP00000507062.1:p.Glu442GlyfsTer9
ENST00000682793.1:c.1324dup	ENSP00000506910.1:p.Glu442GlyfsTer9
ENST00000682838.1:c.*1066dup	ENSP00000507652.1:n.*1066dup
ENST00000683578.1:c.1324dup	ENSP00000507430.1:p.Glu442GlyfsTer9
ENST00000683606.1:n.939dup
ENST00000683661.1:n.2859dup
ENST00000684324.1:c.1324dup	ENSP00000507937.1:p.Glu442GlyfsTer9
ENST00000684545.1:c.1324dup	ENSP00000506733.1:p.Glu442GlyfsTer9
ENST00000684624.1:n.701dup
ENST00000684714.1:c.1324dup	ENSP00000506861.1:p.Glu442GlyfsTer9
ENST00000684731.1:n.785dup
ENST00000375679.9:c.1324dup MANE Select	ENSP00000364831.5:p.Glu442GlyfsTer9
ENST00000375667.7:c.817dup	ENSP00000364819.3:p.Glu273GlyfsTer9
ENST00000375679.8:c.1324dup	ENSP00000364831.4:p.Glu442GlyfsTer9
ENST00000619181.4:c.943dup	ENSP00000483866.1:p.Glu315GlyfsTer9
NM_000085.4:c.1324dup	NP_000076.2:p.Glu442GlyfsTer9
NM_001165945.2:c.817dup	NP_001159417.2:p.Glu273GlyfsTer9
XM_011540619.1:c.1165dup	XP_011538921.1:p.Glu389GlyfsTer9
XM_011540620.1:c.1324dup	XP_011538922.1:p.Glu442GlyfsTer9
XM_011540621.1:c.673dup	XP_011538923.1:p.Glu225GlyfsTer9
NM_000085.5:c.1324dup MANE Select	NP_000076.2:p.Glu442GlyfsTer9