Canonical Allele Identifier: CA1139772942

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16053701T= , CM000663.2:g.16053701T=	GRCh38
NC_000001.10:g.16380196T= , CM000663.1:g.16380196T=	GRCh37
NC_000001.9:g.16252783T=	NCBI36
NG_013079.1:g.14950T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000085.5:c.1685T= MANE Select	NP_000076.2:p.Met562=
ENST00000375679.9:c.1685T= MANE Select	ENSP00000364831.5:p.Met562=
NM_000085.4:c.1685T=	NP_000076.2:p.Met562=
NM_001165945.2:c.1178T=	NP_001159417.2:p.Met393=
ENST00000375667.7:c.1178T=	ENSP00000364819.3:p.Met393=
ENST00000375679.8:c.1685T=	ENSP00000364831.4:p.Met562=
ENST00000431772.1:c.152T=	ENSP00000389344.1:p.Met51=
ENST00000619181.4:c.1293+11T=	ENSP00000483866.1:n.1293+11T=
ENST00000682338.1:c.1685T=	ENSP00000507062.1:p.Met562=
ENST00000682793.1:c.1685T=	ENSP00000506910.1:p.Met562=
ENST00000682838.1:c.*1427T=	ENSP00000507652.1:n.*1427T=
ENST00000683578.1:c.1685T=	ENSP00000507430.1:p.Met562=
ENST00000683606.1:n.1291T=
ENST00000683661.1:n.3220T=
ENST00000684324.1:c.1685T=	ENSP00000507937.1:p.Met562=
ENST00000684545.1:c.1685T=	ENSP00000506733.1:p.Met562=
ENST00000684624.1:n.1062T=
ENST00000684714.1:c.1685T=	ENSP00000506861.1:p.Met562=
ENST00000684731.1:n.1083+1290T=
XM_011540619.1:c.1526T=	XP_011538921.1:p.Met509=
XM_011540621.1:c.1034T=	XP_011538923.1:p.Met345=