Canonical Allele Identifier: CA338641182

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16378033T>G (hg19) ; chr1:g.16051538T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051538T>G , CM000663.2:g.16051538T>G	GRCh38
NC_000001.10:g.16378033T>G , CM000663.1:g.16378033T>G	GRCh37
NC_000001.9:g.16250620T>G	NCBI36
NG_013079.1:g.12787T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1288T>G	ENSP00000507062.1:p.Phe430Val
ENST00000682793.1:c.1288T>G	ENSP00000506910.1:p.Phe430Val
ENST00000682838.1:c.*1030T>G	ENSP00000507652.1:n.*1030T>G
ENST00000683578.1:c.1288T>G	ENSP00000507430.1:p.Phe430Val
ENST00000683606.1:n.903T>G
ENST00000683661.1:n.2823T>G
ENST00000684324.1:c.1288T>G	ENSP00000507937.1:p.Phe430Val
ENST00000684545.1:c.1288T>G	ENSP00000506733.1:p.Phe430Val
ENST00000684624.1:n.665T>G
ENST00000684714.1:c.1288T>G	ENSP00000506861.1:p.Phe430Val
ENST00000684731.1:n.749T>G
ENST00000375679.9:c.1288T>G MANE Select	ENSP00000364831.5:p.Phe430Val
ENST00000375667.7:c.781T>G	ENSP00000364819.3:p.Phe261Val
ENST00000375679.8:c.1288T>G	ENSP00000364831.4:p.Phe430Val
ENST00000619181.4:c.907T>G	ENSP00000483866.1:p.Phe303Val
NM_000085.4:c.1288T>G	NP_000076.2:p.Phe430Val
NM_001165945.2:c.781T>G	NP_001159417.2:p.Phe261Val
XM_011540619.1:c.1129T>G	XP_011538921.1:p.Phe377Val
XM_011540620.1:c.1288T>G	XP_011538922.1:p.Phe430Val
XM_011540621.1:c.637T>G	XP_011538923.1:p.Phe213Val
NM_000085.5:c.1288T>G MANE Select	NP_000076.2:p.Phe430Val