Canonical Allele Identifier: CA890090307

Gene: CLCNKB

Linked Data

• dbSNP Id: rs1245927284
• MyVariant Identifiers: chr1:g.16374961_16374962insG (hg19) ; chr1:g.16048466_16048467insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048471dup , CM000663.2:g.16048471dup	GRCh38
NC_000001.10:g.16374966dup , CM000663.1:g.16374966dup	GRCh37
NC_000001.9:g.16247553dup	NCBI36
NG_013079.1:g.9720dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.577-33dup	ENSP00000507062.1:n.577-33dup
ENST00000682793.1:c.577-33dup	ENSP00000506910.1:n.577-33dup
ENST00000682838.1:c.*235-33dup	ENSP00000507652.1:n.*235-33dup
ENST00000683578.1:c.577-33dup	ENSP00000507430.1:n.577-33dup
ENST00000683661.1:n.2112-33dup
ENST00000684324.1:c.577-33dup	ENSP00000507937.1:n.577-33dup
ENST00000684545.1:c.577-33dup	ENSP00000506733.1:n.577-33dup
ENST00000684714.1:c.577-33dup	ENSP00000506861.1:n.577-33dup
ENST00000684731.1:n.38-33dup
ENST00000375679.9:c.577-33dup MANE Select	ENSP00000364831.5:n.577-33dup
ENST00000375679.8:c.577-33dup	ENSP00000364831.4:n.577-33dup
ENST00000619181.4:c.577-33dup	ENSP00000483866.1:n.577-33dup
NM_000085.4:c.577-33dup	NP_000076.2:n.577-33dup
XM_011540619.1:c.418-33dup	XP_011538921.1:n.418-33dup
XM_011540620.1:c.577-33dup	XP_011538922.1:n.577-33dup
NM_000085.5:c.577-33dup MANE Select	NP_000076.2:n.577-33dup