Canonical Allele Identifier: CA338641950

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16378702C>T (hg19) ; chr1:g.16052207C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052207C>T , CM000663.2:g.16052207C>T	GRCh38
NC_000001.10:g.16378702C>T , CM000663.1:g.16378702C>T	GRCh37
NC_000001.9:g.16251289C>T	NCBI36
NG_013079.1:g.13456C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.1418C>T	ENSP00000507062.1:p.Ala473Val
ENST00000682793.1:c.1418C>T	ENSP00000506910.1:p.Ala473Val
ENST00000682838.1:c.*1160C>T	ENSP00000507652.1:n.*1160C>T
ENST00000683578.1:c.1418C>T	ENSP00000507430.1:p.Ala473Val
ENST00000683606.1:n.1024C>T
ENST00000683661.1:n.2953C>T
ENST00000684324.1:c.1418C>T	ENSP00000507937.1:p.Ala473Val
ENST00000684545.1:c.1418C>T	ENSP00000506733.1:p.Ala473Val
ENST00000684624.1:n.795C>T
ENST00000684714.1:c.1418C>T	ENSP00000506861.1:p.Ala473Val
ENST00000684731.1:n.879C>T
ENST00000375679.9:c.1418C>T MANE Select	ENSP00000364831.5:p.Ala473Val
ENST00000375667.7:c.911C>T	ENSP00000364819.3:p.Ala304Val
ENST00000375679.8:c.1418C>T	ENSP00000364831.4:p.Ala473Val
ENST00000619181.4:c.1037C>T	ENSP00000483866.1:p.Ala346Val
NM_000085.4:c.1418C>T	NP_000076.2:p.Ala473Val
NM_001165945.2:c.911C>T	NP_001159417.2:p.Ala304Val
XM_011540619.1:c.1259C>T	XP_011538921.1:p.Ala420Val
XM_011540620.1:c.1418C>T	XP_011538922.1:p.Ala473Val
XM_011540621.1:c.767C>T	XP_011538923.1:p.Ala256Val
NM_000085.5:c.1418C>T MANE Select	NP_000076.2:p.Ala473Val