Canonical Allele Identifier: CA1155658814

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052205A= , CM000663.2:g.16052205A=	GRCh38
NC_000001.10:g.16378700A= , CM000663.1:g.16378700A=	GRCh37
NC_000001.9:g.16251287A=	NCBI36
NG_013079.1:g.13454A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1416A=	ENSP00000507062.1:p.Ala472=
ENST00000682793.1:c.1416A=	ENSP00000506910.1:p.Ala472=
ENST00000682838.1:c.*1158A=	ENSP00000507652.1:n.*1158A=
ENST00000683578.1:c.1416A=	ENSP00000507430.1:p.Ala472=
ENST00000683606.1:n.1024-2A=
ENST00000683661.1:n.2951A=
ENST00000684324.1:c.1416A=	ENSP00000507937.1:p.Ala472=
ENST00000684545.1:c.1416A=	ENSP00000506733.1:p.Ala472=
ENST00000684624.1:n.793A=
ENST00000684714.1:c.1416A=	ENSP00000506861.1:p.Ala472=
ENST00000684731.1:n.877A=
ENST00000375679.9:c.1416A= MANE Select	ENSP00000364831.5:p.Ala472=
ENST00000375667.7:c.909A=	ENSP00000364819.3:p.Ala303=
ENST00000375679.8:c.1416A=	ENSP00000364831.4:p.Ala472=
ENST00000619181.4:c.1035A=	ENSP00000483866.1:p.Ala345=
NM_000085.4:c.1416A=	NP_000076.2:p.Ala472=
NM_001165945.2:c.909A=	NP_001159417.2:p.Ala303=
XM_011540619.1:c.1257A=	XP_011538921.1:p.Ala419=
XM_011540620.1:c.1416A=	XP_011538922.1:p.Ala472=
XM_011540621.1:c.765A=	XP_011538923.1:p.Ala255=
NM_000085.5:c.1416A= MANE Select	NP_000076.2:p.Ala472=