Canonical Allele Identifier: CA416256448

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16381940C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055445C>A , CM000663.2:g.16055445C>A	GRCh38
NC_000001.10:g.16381940C>A , CM000663.1:g.16381940C>A	GRCh37
NC_000001.9:g.16254527C>A	NCBI36
NG_013079.1:g.16694C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1767C>A	ENSP00000507062.1:p.Ile589=
ENST00000682793.1:c.1767C>A	ENSP00000506910.1:p.Ile589=
ENST00000682838.1:c.*1509C>A	ENSP00000507652.1:n.*1509C>A
ENST00000683578.1:c.1767C>A	ENSP00000507430.1:p.Ile589=
ENST00000683606.1:n.1373C>A
ENST00000683661.1:n.3302C>A
ENST00000684324.1:c.1767C>A	ENSP00000507937.1:p.Ile589=
ENST00000684545.1:c.1767C>A	ENSP00000506733.1:p.Ile589=
ENST00000684624.1:n.1144C>A
ENST00000684714.1:c.1718C>A	ENSP00000506861.1:p.Ser573Tyr
ENST00000684731.1:n.1094C>A
ENST00000375679.9:c.1767C>A MANE Select	ENSP00000364831.5:p.Ile589=
ENST00000375667.7:c.1260C>A	ENSP00000364819.3:p.Ile420=
ENST00000375679.8:c.1767C>A	ENSP00000364831.4:p.Ile589=
ENST00000431772.1:c.234C>A	ENSP00000389344.1:p.Ile78=
ENST00000619181.4:c.1294-1742C>A	ENSP00000483866.1:n.1294-1742C>A
NM_000085.4:c.1767C>A	NP_000076.2:p.Ile589=
NM_001165945.2:c.1260C>A	NP_001159417.2:p.Ile420=
XM_011540619.1:c.1608C>A	XP_011538921.1:p.Ile536=
XM_011540621.1:c.1116C>A	XP_011538923.1:p.Ile372=
NM_000085.5:c.1767C>A MANE Select	NP_000076.2:p.Ile589=