Canonical Allele Identifier: CA1155658812

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052199G= , CM000663.2:g.16052199G=	GRCh38
NC_000001.10:g.16378694G= , CM000663.1:g.16378694G=	GRCh37
NC_000001.9:g.16251281G=	NCBI36
NG_013079.1:g.13448G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.1410G=	ENSP00000507062.1:p.Gly470=
ENST00000682793.1:c.1410G=	ENSP00000506910.1:p.Gly470=
ENST00000682838.1:c.*1152G=	ENSP00000507652.1:n.*1152G=
ENST00000683578.1:c.1410G=	ENSP00000507430.1:p.Gly470=
ENST00000683606.1:n.1024-8G=
ENST00000683661.1:n.2945G=
ENST00000684324.1:c.1410G=	ENSP00000507937.1:p.Gly470=
ENST00000684545.1:c.1410G=	ENSP00000506733.1:p.Gly470=
ENST00000684624.1:n.787G=
ENST00000684714.1:c.1410G=	ENSP00000506861.1:p.Gly470=
ENST00000684731.1:n.871G=
ENST00000375679.9:c.1410G= MANE Select	ENSP00000364831.5:p.Gly470=
ENST00000375667.7:c.903G=	ENSP00000364819.3:p.Gly301=
ENST00000375679.8:c.1410G=	ENSP00000364831.4:p.Gly470=
ENST00000619181.4:c.1029G=	ENSP00000483866.1:p.Gly343=
NM_000085.4:c.1410G=	NP_000076.2:p.Gly470=
NM_001165945.2:c.903G=	NP_001159417.2:p.Gly301=
XM_011540619.1:c.1251G=	XP_011538921.1:p.Gly417=
XM_011540620.1:c.1410G=	XP_011538922.1:p.Gly470=
XM_011540621.1:c.759G=	XP_011538923.1:p.Gly253=
NM_000085.5:c.1410G= MANE Select	NP_000076.2:p.Gly470=