Canonical Allele Identifier: CA1155655552

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048556C= , CM000663.2:g.16048556C=	GRCh38
NC_000001.10:g.16375051C= , CM000663.1:g.16375051C=	GRCh37
NC_000001.9:g.16247638C=	NCBI36
NG_013079.1:g.9805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.629C=	ENSP00000507062.1:p.Ala210=
ENST00000682793.1:c.629C=	ENSP00000506910.1:p.Ala210=
ENST00000682838.1:c.*287C=	ENSP00000507652.1:n.*287C=
ENST00000683578.1:c.629C=	ENSP00000507430.1:p.Ala210=
ENST00000683661.1:n.2164C=
ENST00000684324.1:c.629C=	ENSP00000507937.1:p.Ala210=
ENST00000684545.1:c.629C=	ENSP00000506733.1:p.Ala210=
ENST00000684714.1:c.629C=	ENSP00000506861.1:p.Ala210=
ENST00000684731.1:n.90C=
ENST00000375679.9:c.629C= MANE Select	ENSP00000364831.5:p.Ala210=
ENST00000375679.8:c.629C=	ENSP00000364831.4:p.Ala210=
ENST00000619181.4:c.587+42C=	ENSP00000483866.1:n.587+42C=
NM_000085.4:c.629C=	NP_000076.2:p.Ala210=
XM_011540619.1:c.470C=	XP_011538921.1:p.Ala157=
XM_011540620.1:c.629C=	XP_011538922.1:p.Ala210=
NM_000085.5:c.629C= MANE Select	NP_000076.2:p.Ala210=