Canonical Allele Identifier: CA338641362

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16378228G>C (hg19) ; chr1:g.16051733G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051733G>C , CM000663.2:g.16051733G>C	GRCh38
NC_000001.10:g.16378228G>C , CM000663.1:g.16378228G>C	GRCh37
NC_000001.9:g.16250815G>C	NCBI36
NG_013079.1:g.12982G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1321G>C	ENSP00000507062.1:p.Gly441Arg
ENST00000682793.1:c.1321G>C	ENSP00000506910.1:p.Gly441Arg
ENST00000682838.1:c.*1063G>C	ENSP00000507652.1:n.*1063G>C
ENST00000683578.1:c.1321G>C	ENSP00000507430.1:p.Gly441Arg
ENST00000683606.1:n.936G>C
ENST00000683661.1:n.2856G>C
ENST00000684324.1:c.1321G>C	ENSP00000507937.1:p.Gly441Arg
ENST00000684545.1:c.1321G>C	ENSP00000506733.1:p.Gly441Arg
ENST00000684624.1:n.698G>C
ENST00000684714.1:c.1321G>C	ENSP00000506861.1:p.Gly441Arg
ENST00000684731.1:n.782G>C
ENST00000375679.9:c.1321G>C MANE Select	ENSP00000364831.5:p.Gly441Arg
ENST00000375667.7:c.814G>C	ENSP00000364819.3:p.Gly272Arg
ENST00000375679.8:c.1321G>C	ENSP00000364831.4:p.Gly441Arg
ENST00000619181.4:c.940G>C	ENSP00000483866.1:p.Gly314Arg
NM_000085.4:c.1321G>C	NP_000076.2:p.Gly441Arg
NM_001165945.2:c.814G>C	NP_001159417.2:p.Gly272Arg
XM_011540619.1:c.1162G>C	XP_011538921.1:p.Gly388Arg
XM_011540620.1:c.1321G>C	XP_011538922.1:p.Gly441Arg
XM_011540621.1:c.670G>C	XP_011538923.1:p.Gly224Arg
NM_000085.5:c.1321G>C MANE Select	NP_000076.2:p.Gly441Arg