Canonical Allele Identifier: CA1155655803

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048688T= , CM000663.2:g.16048688T=	GRCh38
NC_000001.10:g.16375183T= , CM000663.1:g.16375183T=	GRCh37
NC_000001.9:g.16247770T=	NCBI36
NG_013079.1:g.9937T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.655+106T=	ENSP00000507062.1:n.655+106T=
ENST00000682793.1:c.655+106T=	ENSP00000506910.1:n.655+106T=
ENST00000682838.1:c.*313+106T=	ENSP00000507652.1:n.*313+106T=
ENST00000683578.1:c.655+106T=	ENSP00000507430.1:n.655+106T=
ENST00000683661.1:n.2190+106T=
ENST00000684324.1:c.655+106T=	ENSP00000507937.1:n.655+106T=
ENST00000684545.1:c.655+106T=	ENSP00000506733.1:n.655+106T=
ENST00000684714.1:c.655+106T=	ENSP00000506861.1:n.655+106T=
ENST00000684731.1:n.116+106T=
ENST00000375679.9:c.655+106T= MANE Select	ENSP00000364831.5:n.655+106T=
ENST00000375679.8:c.655+106T=	ENSP00000364831.4:n.655+106T=
ENST00000619181.4:c.587+174T=	ENSP00000483866.1:n.587+174T=
NM_000085.4:c.655+106T=	NP_000076.2:n.655+106T=
XM_011540619.1:c.496+106T=	XP_011538921.1:n.496+106T=
XM_011540620.1:c.655+106T=	XP_011538922.1:n.655+106T=
NM_000085.5:c.655+106T= MANE Select	NP_000076.2:n.655+106T=