Canonical Allele Identifier: CA416256511

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16381958A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055463A>T , CM000663.2:g.16055463A>T	GRCh38
NC_000001.10:g.16381958A>T , CM000663.1:g.16381958A>T	GRCh37
NC_000001.9:g.16254545A>T	NCBI36
NG_013079.1:g.16712A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1785A>T	ENSP00000507062.1:p.Arg595=
ENST00000682793.1:c.1785A>T	ENSP00000506910.1:p.Arg595=
ENST00000682838.1:c.*1527A>T	ENSP00000507652.1:n.*1527A>T
ENST00000683578.1:c.1785A>T	ENSP00000507430.1:p.Arg595=
ENST00000683606.1:n.1391A>T
ENST00000683661.1:n.3320A>T
ENST00000684324.1:c.1785A>T	ENSP00000507937.1:p.Arg595=
ENST00000684545.1:c.1785A>T	ENSP00000506733.1:p.Arg595=
ENST00000684624.1:n.1162A>T
ENST00000684714.1:c.*5A>T	ENSP00000506861.1:n.*5A>T
ENST00000684731.1:n.1112A>T
ENST00000375679.9:c.1785A>T MANE Select	ENSP00000364831.5:p.Arg595=
ENST00000375667.7:c.1278A>T	ENSP00000364819.3:p.Arg426=
ENST00000375679.8:c.1785A>T	ENSP00000364831.4:p.Arg595=
ENST00000431772.1:c.252A>T	ENSP00000389344.1:p.Arg84=
ENST00000619181.4:c.1294-1724A>T	ENSP00000483866.1:n.1294-1724A>T
NM_000085.4:c.1785A>T	NP_000076.2:p.Arg595=
NM_001165945.2:c.1278A>T	NP_001159417.2:p.Arg426=
XM_011540619.1:c.1626A>T	XP_011538921.1:p.Arg542=
XM_011540621.1:c.1134A>T	XP_011538923.1:p.Arg378=
NM_000085.5:c.1785A>T MANE Select	NP_000076.2:p.Arg595=