Canonical Allele Identifier: CA1155617773

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055449G= , CM000663.2:g.16055449G=	GRCh38
NC_000001.10:g.16381944G= , CM000663.1:g.16381944G=	GRCh37
NC_000001.9:g.16254531G=	NCBI36
NG_013079.1:g.16698G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1771G=	ENSP00000507062.1:p.Val591=
ENST00000682793.1:c.1771G=	ENSP00000506910.1:p.Val591=
ENST00000682838.1:c.*1513G=	ENSP00000507652.1:n.*1513G=
ENST00000683578.1:c.1771G=	ENSP00000507430.1:p.Val591=
ENST00000683606.1:n.1377G=
ENST00000683661.1:n.3306G=
ENST00000684324.1:c.1771G=	ENSP00000507937.1:p.Val591=
ENST00000684545.1:c.1771G=	ENSP00000506733.1:p.Val591=
ENST00000684624.1:n.1148G=
ENST00000684714.1:c.1722G=	ENSP00000506861.1:p.Trp574=
ENST00000684731.1:n.1098G=
ENST00000375679.9:c.1771G= MANE Select	ENSP00000364831.5:p.Val591=
ENST00000375667.7:c.1264G=	ENSP00000364819.3:p.Val422=
ENST00000375679.8:c.1771G=	ENSP00000364831.4:p.Val591=
ENST00000431772.1:c.238G=	ENSP00000389344.1:p.Val80=
ENST00000619181.4:c.1294-1738G=	ENSP00000483866.1:n.1294-1738G=
NM_000085.4:c.1771G=	NP_000076.2:p.Val591=
NM_001165945.2:c.1264G=	NP_001159417.2:p.Val422=
XM_011540619.1:c.1612G=	XP_011538921.1:p.Val538=
XM_011540621.1:c.1120G=	XP_011538923.1:p.Val374=
NM_000085.5:c.1771G= MANE Select	NP_000076.2:p.Val591=