Canonical Allele Identifier: CA1155617855

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055480A= , CM000663.2:g.16055480A=	GRCh38
NC_000001.10:g.16381975A= , CM000663.1:g.16381975A=	GRCh37
NC_000001.9:g.16254562A=	NCBI36
NG_013079.1:g.16729A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1802A=	ENSP00000507062.1:p.Gln601=
ENST00000682793.1:c.1802A=	ENSP00000506910.1:p.Gln601=
ENST00000682838.1:c.*1544A=	ENSP00000507652.1:n.*1544A=
ENST00000683578.1:c.1802A=	ENSP00000507430.1:p.Gln601=
ENST00000683606.1:n.1408A=
ENST00000683661.1:n.3337A=
ENST00000684324.1:c.1802A=	ENSP00000507937.1:p.Gln601=
ENST00000684545.1:c.1802A=	ENSP00000506733.1:p.Gln601=
ENST00000684624.1:n.1179A=
ENST00000684714.1:c.*22A=	ENSP00000506861.1:n.*22A=
ENST00000684731.1:n.1129A=
ENST00000375679.9:c.1802A= MANE Select	ENSP00000364831.5:p.Gln601=
ENST00000375667.7:c.1295A=	ENSP00000364819.3:p.Gln432=
ENST00000375679.8:c.1802A=	ENSP00000364831.4:p.Gln601=
ENST00000431772.1:c.269A=	ENSP00000389344.1:p.Gln90=
ENST00000619181.4:c.1294-1707A=	ENSP00000483866.1:n.1294-1707A=
NM_000085.4:c.1802A=	NP_000076.2:p.Gln601=
NM_001165945.2:c.1295A=	NP_001159417.2:p.Gln432=
XM_011540619.1:c.1643A=	XP_011538921.1:p.Gln548=
XM_011540621.1:c.1151A=	XP_011538923.1:p.Gln384=
NM_000085.5:c.1802A= MANE Select	NP_000076.2:p.Gln601=