Canonical Allele Identifier: CA338644749

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16381972T>A (hg19) ; chr1:g.16055477T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055477T>A , CM000663.2:g.16055477T>A	GRCh38
NC_000001.10:g.16381972T>A , CM000663.1:g.16381972T>A	GRCh37
NC_000001.9:g.16254559T>A	NCBI36
NG_013079.1:g.16726T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1799T>A	ENSP00000507062.1:p.Val600Glu
ENST00000682793.1:c.1799T>A	ENSP00000506910.1:p.Val600Glu
ENST00000682838.1:c.*1541T>A	ENSP00000507652.1:n.*1541T>A
ENST00000683578.1:c.1799T>A	ENSP00000507430.1:p.Val600Glu
ENST00000683606.1:n.1405T>A
ENST00000683661.1:n.3334T>A
ENST00000684324.1:c.1799T>A	ENSP00000507937.1:p.Val600Glu
ENST00000684545.1:c.1799T>A	ENSP00000506733.1:p.Val600Glu
ENST00000684624.1:n.1176T>A
ENST00000684714.1:c.*19T>A	ENSP00000506861.1:n.*19T>A
ENST00000684731.1:n.1126T>A
ENST00000375679.9:c.1799T>A MANE Select	ENSP00000364831.5:p.Val600Glu
ENST00000375667.7:c.1292T>A	ENSP00000364819.3:p.Val431Glu
ENST00000375679.8:c.1799T>A	ENSP00000364831.4:p.Val600Glu
ENST00000431772.1:c.266T>A	ENSP00000389344.1:p.Val89Glu
ENST00000619181.4:c.1294-1710T>A	ENSP00000483866.1:n.1294-1710T>A
NM_000085.4:c.1799T>A	NP_000076.2:p.Val600Glu
NM_001165945.2:c.1292T>A	NP_001159417.2:p.Val431Glu
XM_011540619.1:c.1640T>A	XP_011538921.1:p.Val547Glu
XM_011540621.1:c.1148T>A	XP_011538923.1:p.Val383Glu
NM_000085.5:c.1799T>A MANE Select	NP_000076.2:p.Val600Glu