Canonical Allele Identifier: CA1155655942

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048780C= , CM000663.2:g.16048780C=	GRCh38
NC_000001.10:g.16375275C= , CM000663.1:g.16375275C=	GRCh37
NC_000001.9:g.16247862C=	NCBI36
NG_013079.1:g.10029C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.655+198C=	ENSP00000507062.1:n.655+198C=
ENST00000682793.1:c.655+198C=	ENSP00000506910.1:n.655+198C=
ENST00000682838.1:c.*313+198C=	ENSP00000507652.1:n.*313+198C=
ENST00000683578.1:c.655+198C=	ENSP00000507430.1:n.655+198C=
ENST00000683661.1:n.2190+198C=
ENST00000684324.1:c.655+198C=	ENSP00000507937.1:n.655+198C=
ENST00000684545.1:c.655+198C=	ENSP00000506733.1:n.655+198C=
ENST00000684714.1:c.655+198C=	ENSP00000506861.1:n.655+198C=
ENST00000684731.1:n.116+198C=
ENST00000375679.9:c.655+198C= MANE Select	ENSP00000364831.5:n.655+198C=
ENST00000375679.8:c.655+198C=	ENSP00000364831.4:n.655+198C=
ENST00000619181.4:c.587+266C=	ENSP00000483866.1:n.587+266C=
NM_000085.4:c.655+198C=	NP_000076.2:n.655+198C=
NM_001165945.2:c.-192C=	NP_001159417.2:n.-192C=
XM_011540619.1:c.496+198C=	XP_011538921.1:n.496+198C=
XM_011540620.1:c.655+198C=	XP_011538922.1:n.655+198C=
XM_011540621.1:c.-248C=	XP_011538923.1:n.-248C=
NM_000085.5:c.655+198C= MANE Select	NP_000076.2:n.655+198C=