Canonical Allele Identifier: CA416256669

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16382000C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055505C>A , CM000663.2:g.16055505C>A	GRCh38
NC_000001.10:g.16382000C>A , CM000663.1:g.16382000C>A	GRCh37
NC_000001.9:g.16254587C>A	NCBI36
NG_013079.1:g.16754C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1827C>A	ENSP00000507062.1:p.Ser609=
ENST00000682793.1:c.1827C>A	ENSP00000506910.1:p.Ser609=
ENST00000682838.1:c.*1569C>A	ENSP00000507652.1:n.*1569C>A
ENST00000683578.1:c.1827C>A	ENSP00000507430.1:p.Ser609=
ENST00000683606.1:n.1433C>A
ENST00000683661.1:n.3362C>A
ENST00000684324.1:c.1827C>A	ENSP00000507937.1:p.Ser609=
ENST00000684545.1:c.1827C>A	ENSP00000506733.1:p.Ser609=
ENST00000684624.1:n.1204C>A
ENST00000684714.1:c.*47C>A	ENSP00000506861.1:n.*47C>A
ENST00000684731.1:n.1154C>A
ENST00000375679.9:c.1827C>A MANE Select	ENSP00000364831.5:p.Ser609=
ENST00000375667.7:c.1320C>A	ENSP00000364819.3:p.Ser440=
ENST00000375679.8:c.1827C>A	ENSP00000364831.4:p.Ser609=
ENST00000431772.1:c.294C>A	ENSP00000389344.1:p.Ser98=
ENST00000619181.4:c.1294-1682C>A	ENSP00000483866.1:n.1294-1682C>A
NM_000085.4:c.1827C>A	NP_000076.2:p.Ser609=
NM_001165945.2:c.1320C>A	NP_001159417.2:p.Ser440=
XM_011540619.1:c.1668C>A	XP_011538921.1:p.Ser556=
XM_011540621.1:c.1176C>A	XP_011538923.1:p.Ser392=
NM_000085.5:c.1827C>A MANE Select	NP_000076.2:p.Ser609=