Canonical Allele Identifier: CA1139907430

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16044572G= , CM000663.2:g.16044572G=	GRCh38
NC_000001.10:g.16371067G= , CM000663.1:g.16371067G=	GRCh37
NC_000001.9:g.16243654G=	NCBI36
NG_013079.1:g.5821G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000085.5:c.80G= MANE Select	NP_000076.2:p.Arg27=
ENST00000375679.9:c.80G= MANE Select	ENSP00000364831.5:p.Arg27=
NM_000085.4:c.80G=	NP_000076.2:p.Arg27=
ENST00000375679.8:c.80G=	ENSP00000364831.4:p.Arg27=
ENST00000619181.4:c.80G=	ENSP00000483866.1:p.Arg27=
ENST00000682338.1:c.80G=	ENSP00000507062.1:p.Arg27=
ENST00000682793.1:c.80G=	ENSP00000506910.1:p.Arg27=
ENST00000682838.1:c.80G=	ENSP00000507652.1:p.Arg27=
ENST00000683578.1:c.80G=	ENSP00000507430.1:p.Arg27=
ENST00000684324.1:c.80G=	ENSP00000507937.1:p.Arg27=
ENST00000684545.1:c.80G=	ENSP00000506733.1:p.Arg27=
ENST00000684714.1:c.80G=	ENSP00000506861.1:p.Arg27=
XM_011540619.1:c.-301G=	XP_011538921.1:n.-301G=
XM_011540620.1:c.80G=	XP_011538922.1:p.Arg27=