Canonical Allele Identifier: CA338645790

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055759G>A , CM000663.2:g.16055759G>A	GRCh38
NC_000001.10:g.16382254G>A , CM000663.1:g.16382254G>A	GRCh37
NC_000001.9:g.16254841G>A	NCBI36
NG_013079.1:g.17008G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000085.5:c.1929+1G>A MANE Select	NP_000076.2:n.1929+1G>A
ENST00000375679.9:c.1929+1G>A MANE Select	ENSP00000364831.5:n.1929+1G>A
NM_000085.4:c.1929+1G>A	NP_000076.2:n.1929+1G>A
NM_001165945.2:c.1419+1G>A	NP_001159417.2:n.1419+1G>A
ENST00000375667.7:c.1419+1G>A	ENSP00000364819.3:n.1419+1G>A
ENST00000375679.8:c.1929+1G>A	ENSP00000364831.4:n.1929+1G>A
ENST00000431772.1:c.393+1G>A	ENSP00000389344.1:n.393+1G>A
ENST00000619181.4:c.1294-1428G>A	ENSP00000483866.1:n.1294-1428G>A
ENST00000682338.1:c.1929+1G>A	ENSP00000507062.1:n.1929+1G>A
ENST00000682793.1:c.1929+1G>A	ENSP00000506910.1:n.1929+1G>A
ENST00000682838.1:c.*1668+1G>A	ENSP00000507652.1:n.*1668+1G>A
ENST00000683578.1:c.1926+1G>A	ENSP00000507430.1:n.1926+1G>A
ENST00000683606.1:n.1532+1G>A
ENST00000683661.1:n.3464+1G>A
ENST00000684324.1:c.1929+1G>A	ENSP00000507937.1:n.1929+1G>A
ENST00000684545.1:c.1929+1G>A	ENSP00000506733.1:n.1929+1G>A
ENST00000684624.1:n.1306+1G>A
ENST00000684714.1:c.*149+1G>A	ENSP00000506861.1:n.*149+1G>A
ENST00000684731.1:n.1256+1G>A
XM_011540619.1:c.1770+1G>A	XP_011538921.1:n.1770+1G>A
XM_011540621.1:c.1278+1G>A	XP_011538923.1:n.1278+1G>A