Canonical Allele Identifier: CA1139925381

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16053748A= , CM000663.2:g.16053748A=	GRCh38
NC_000001.10:g.16380243A= , CM000663.1:g.16380243A=	GRCh37
NC_000001.9:g.16252830A=	NCBI36
NG_013079.1:g.14997A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1732A=	ENSP00000507062.1:p.Lys578=
ENST00000682793.1:c.1732A=	ENSP00000506910.1:p.Lys578=
ENST00000682838.1:c.*1474A=	ENSP00000507652.1:n.*1474A=
ENST00000683578.1:c.1732A=	ENSP00000507430.1:p.Lys578=
ENST00000683606.1:n.1338A=
ENST00000683661.1:n.3267A=
ENST00000684324.1:c.1732A=	ENSP00000507937.1:p.Lys578=
ENST00000684545.1:c.1732A=	ENSP00000506733.1:p.Lys578=
ENST00000684624.1:n.1109A=
ENST00000684714.1:c.1707+25A=	ENSP00000506861.1:n.1707+25A=
ENST00000684731.1:n.1083+1337A=
ENST00000375679.9:c.1732A= MANE Select	ENSP00000364831.5:p.Lys578=
ENST00000375667.7:c.1225A=	ENSP00000364819.3:p.Lys409=
ENST00000375679.8:c.1732A=	ENSP00000364831.4:p.Lys578=
ENST00000431772.1:c.199A=	ENSP00000389344.1:p.Lys67=
ENST00000619181.4:c.1293+58A=	ENSP00000483866.1:n.1293+58A=
NM_000085.4:c.1732A=	NP_000076.2:p.Lys578=
NM_001165945.2:c.1225A=	NP_001159417.2:p.Lys409=
XM_011540619.1:c.1573A=	XP_011538921.1:p.Lys525=
XM_011540621.1:c.1081A=	XP_011538923.1:p.Lys361=
NM_000085.5:c.1732A= MANE Select	NP_000076.2:p.Lys578=