Canonical Allele Identifier: CA338641366

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16378229G>T (hg19) ; chr1:g.16051734G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051734G>T , CM000663.2:g.16051734G>T	GRCh38
NC_000001.10:g.16378229G>T , CM000663.1:g.16378229G>T	GRCh37
NC_000001.9:g.16250816G>T	NCBI36
NG_013079.1:g.12983G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1322G>T	ENSP00000507062.1:p.Gly441Val
ENST00000682793.1:c.1322G>T	ENSP00000506910.1:p.Gly441Val
ENST00000682838.1:c.*1064G>T	ENSP00000507652.1:n.*1064G>T
ENST00000683578.1:c.1322G>T	ENSP00000507430.1:p.Gly441Val
ENST00000683606.1:n.937G>T
ENST00000683661.1:n.2857G>T
ENST00000684324.1:c.1322G>T	ENSP00000507937.1:p.Gly441Val
ENST00000684545.1:c.1322G>T	ENSP00000506733.1:p.Gly441Val
ENST00000684624.1:n.699G>T
ENST00000684714.1:c.1322G>T	ENSP00000506861.1:p.Gly441Val
ENST00000684731.1:n.783G>T
ENST00000375679.9:c.1322G>T MANE Select	ENSP00000364831.5:p.Gly441Val
ENST00000375667.7:c.815G>T	ENSP00000364819.3:p.Gly272Val
ENST00000375679.8:c.1322G>T	ENSP00000364831.4:p.Gly441Val
ENST00000619181.4:c.941G>T	ENSP00000483866.1:p.Gly314Val
NM_000085.4:c.1322G>T	NP_000076.2:p.Gly441Val
NM_001165945.2:c.815G>T	NP_001159417.2:p.Gly272Val
XM_011540619.1:c.1163G>T	XP_011538921.1:p.Gly388Val
XM_011540620.1:c.1322G>T	XP_011538922.1:p.Gly441Val
XM_011540621.1:c.671G>T	XP_011538923.1:p.Gly224Val
NM_000085.5:c.1322G>T MANE Select	NP_000076.2:p.Gly441Val