Canonical Allele Identifier: CA338641348

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16378225T>G (hg19) ; chr1:g.16051730T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051730T>G , CM000663.2:g.16051730T>G	GRCh38
NC_000001.10:g.16378225T>G , CM000663.1:g.16378225T>G	GRCh37
NC_000001.9:g.16250812T>G	NCBI36
NG_013079.1:g.12979T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1318T>G	ENSP00000507062.1:p.Phe440Val
ENST00000682793.1:c.1318T>G	ENSP00000506910.1:p.Phe440Val
ENST00000682838.1:c.*1060T>G	ENSP00000507652.1:n.*1060T>G
ENST00000683578.1:c.1318T>G	ENSP00000507430.1:p.Phe440Val
ENST00000683606.1:n.933T>G
ENST00000683661.1:n.2853T>G
ENST00000684324.1:c.1318T>G	ENSP00000507937.1:p.Phe440Val
ENST00000684545.1:c.1318T>G	ENSP00000506733.1:p.Phe440Val
ENST00000684624.1:n.695T>G
ENST00000684714.1:c.1318T>G	ENSP00000506861.1:p.Phe440Val
ENST00000684731.1:n.779T>G
ENST00000375679.9:c.1318T>G MANE Select	ENSP00000364831.5:p.Phe440Val
ENST00000375667.7:c.811T>G	ENSP00000364819.3:p.Phe271Val
ENST00000375679.8:c.1318T>G	ENSP00000364831.4:p.Phe440Val
ENST00000619181.4:c.937T>G	ENSP00000483866.1:p.Phe313Val
NM_000085.4:c.1318T>G	NP_000076.2:p.Phe440Val
NM_001165945.2:c.811T>G	NP_001159417.2:p.Phe271Val
XM_011540619.1:c.1159T>G	XP_011538921.1:p.Phe387Val
XM_011540620.1:c.1318T>G	XP_011538922.1:p.Phe440Val
XM_011540621.1:c.667T>G	XP_011538923.1:p.Phe223Val
NM_000085.5:c.1318T>G MANE Select	NP_000076.2:p.Phe440Val