Canonical Allele Identifier: CA1141580608

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051724C= , CM000663.2:g.16051724C=	GRCh38
NC_000001.10:g.16378219C= , CM000663.1:g.16378219C=	GRCh37
NC_000001.9:g.16250806C=	NCBI36
NG_013079.1:g.12973C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1312C=	ENSP00000507062.1:p.Arg438=
ENST00000682793.1:c.1312C=	ENSP00000506910.1:p.Arg438=
ENST00000682838.1:c.*1054C=	ENSP00000507652.1:n.*1054C=
ENST00000683578.1:c.1312C=	ENSP00000507430.1:p.Arg438=
ENST00000683606.1:n.927C=
ENST00000683661.1:n.2847C=
ENST00000684324.1:c.1312C=	ENSP00000507937.1:p.Arg438=
ENST00000684545.1:c.1312C=	ENSP00000506733.1:p.Arg438=
ENST00000684624.1:n.689C=
ENST00000684714.1:c.1312C=	ENSP00000506861.1:p.Arg438=
ENST00000684731.1:n.773C=
ENST00000375679.9:c.1312C= MANE Select	ENSP00000364831.5:p.Arg438=
ENST00000375667.7:c.805C=	ENSP00000364819.3:p.Arg269=
ENST00000375679.8:c.1312C=	ENSP00000364831.4:p.Arg438=
ENST00000619181.4:c.931C=	ENSP00000483866.1:p.Arg311=
NM_000085.4:c.1312C=	NP_000076.2:p.Arg438=
NM_001165945.2:c.805C=	NP_001159417.2:p.Arg269=
XM_011540619.1:c.1153C=	XP_011538921.1:p.Arg385=
XM_011540620.1:c.1312C=	XP_011538922.1:p.Arg438=
XM_011540621.1:c.661C=	XP_011538923.1:p.Arg221=
NM_000085.5:c.1312C= MANE Select	NP_000076.2:p.Arg438=