Canonical Allele Identifier: CA2574230796

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051643C>A , CM000663.2:g.16051643C>A	GRCh38
NC_000001.10:g.16378138C>A , CM000663.1:g.16378138C>A	GRCh37
NC_000001.9:g.16250725C>A	NCBI36
NG_013079.1:g.12892C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1298-67C>A	ENSP00000507062.1:n.1298-67C>A
ENST00000682793.1:c.1298-67C>A	ENSP00000506910.1:n.1298-67C>A
ENST00000682838.1:c.*1040-67C>A	ENSP00000507652.1:n.*1040-67C>A
ENST00000683578.1:c.1298-67C>A	ENSP00000507430.1:n.1298-67C>A
ENST00000683606.1:n.913-67C>A
ENST00000683661.1:n.2833-67C>A
ENST00000684324.1:c.1298-67C>A	ENSP00000507937.1:n.1298-67C>A
ENST00000684545.1:c.1298-67C>A	ENSP00000506733.1:n.1298-67C>A
ENST00000684624.1:n.675-67C>A
ENST00000684714.1:c.1298-67C>A	ENSP00000506861.1:n.1298-67C>A
ENST00000684731.1:n.759-67C>A
ENST00000375679.9:c.1298-67C>A MANE Select	ENSP00000364831.5:n.1298-67C>A
ENST00000375667.7:c.791-67C>A	ENSP00000364819.3:n.791-67C>A
ENST00000375679.8:c.1298-67C>A	ENSP00000364831.4:n.1298-67C>A
ENST00000619181.4:c.917-67C>A	ENSP00000483866.1:n.917-67C>A
NM_000085.4:c.1298-67C>A	NP_000076.2:n.1298-67C>A
NM_001165945.2:c.791-67C>A	NP_001159417.2:n.791-67C>A
XM_011540619.1:c.1139-67C>A	XP_011538921.1:n.1139-67C>A
XM_011540620.1:c.1298-67C>A	XP_011538922.1:n.1298-67C>A
XM_011540621.1:c.647-67C>A	XP_011538923.1:n.647-67C>A
NM_000085.5:c.1298-67C>A MANE Select	NP_000076.2:n.1298-67C>A