Canonical Allele Identifier: CA1155658820

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052218G= , CM000663.2:g.16052218G=	GRCh38
NC_000001.10:g.16378713G= , CM000663.1:g.16378713G=	GRCh37
NC_000001.9:g.16251300G=	NCBI36
NG_013079.1:g.13467G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1429G=	ENSP00000507062.1:p.Ala477=
ENST00000682793.1:c.1429G=	ENSP00000506910.1:p.Ala477=
ENST00000682838.1:c.*1171G=	ENSP00000507652.1:n.*1171G=
ENST00000683578.1:c.1429G=	ENSP00000507430.1:p.Ala477=
ENST00000683606.1:n.1035G=
ENST00000683661.1:n.2964G=
ENST00000684324.1:c.1429G=	ENSP00000507937.1:p.Ala477=
ENST00000684545.1:c.1429G=	ENSP00000506733.1:p.Ala477=
ENST00000684624.1:n.806G=
ENST00000684714.1:c.1429G=	ENSP00000506861.1:p.Ala477=
ENST00000684731.1:n.890G=
ENST00000375679.9:c.1429G= MANE Select	ENSP00000364831.5:p.Ala477=
ENST00000375667.7:c.922G=	ENSP00000364819.3:p.Ala308=
ENST00000375679.8:c.1429G=	ENSP00000364831.4:p.Ala477=
ENST00000619181.4:c.1048G=	ENSP00000483866.1:p.Ala350=
NM_000085.4:c.1429G=	NP_000076.2:p.Ala477=
NM_001165945.2:c.922G=	NP_001159417.2:p.Ala308=
XM_011540619.1:c.1270G=	XP_011538921.1:p.Ala424=
XM_011540620.1:c.1429G=	XP_011538922.1:p.Ala477=
XM_011540621.1:c.778G=	XP_011538923.1:p.Ala260=
NM_000085.5:c.1429G= MANE Select	NP_000076.2:p.Ala477=