Canonical Allele Identifier: CA2643565272

Gene: CLCNKB

Linked Data

• dbSNP Id: rs2124111128
• gnomAD v4: 1-16055547-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055548_16055549del , CM000663.2:g.16055548_16055549del	GRCh38
NC_000001.10:g.16382043_16382044del , CM000663.1:g.16382043_16382044del	GRCh37
NC_000001.9:g.16254630_16254631del	NCBI36
NG_013079.1:g.16797_16798del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1845+25_1845+26del	ENSP00000507062.1:n.1845+25_1845+26del
ENST00000682793.1:c.1845+25_1845+26del	ENSP00000506910.1:n.1845+25_1845+26del
ENST00000682838.1:c.*1587+25_*1587+26del	ENSP00000507652.1:n.*1587+25_*1587+26del
ENST00000683578.1:c.1845+25_1845+26del	ENSP00000507430.1:n.1845+25_1845+26del
ENST00000683606.1:n.1451+25_1451+26del
ENST00000683661.1:n.3380+25_3380+26del
ENST00000684324.1:c.1845+25_1845+26del	ENSP00000507937.1:n.1845+25_1845+26del
ENST00000684545.1:c.1845+25_1845+26del	ENSP00000506733.1:n.1845+25_1845+26del
ENST00000684624.1:n.1222+25_1222+26del
ENST00000684714.1:c.*65+25_*65+26del	ENSP00000506861.1:n.*65+25_*65+26del
ENST00000684731.1:n.1172+25_1172+26del
ENST00000375679.9:c.1845+25_1845+26del MANE Select	ENSP00000364831.5:n.1845+25_1845+26del
ENST00000375667.7:c.1338+25_1338+26del	ENSP00000364819.3:n.1338+25_1338+26del
ENST00000375679.8:c.1845+25_1845+26del	ENSP00000364831.4:n.1845+25_1845+26del
ENST00000431772.1:c.312+25_312+26del	ENSP00000389344.1:n.312+25_312+26del
ENST00000619181.4:c.1294-1639_1294-1638del	ENSP00000483866.1:n.1294-1639_1294-1638del
NM_000085.4:c.1845+25_1845+26del	NP_000076.2:n.1845+25_1845+26del
NM_001165945.2:c.1338+25_1338+26del	NP_001159417.2:n.1338+25_1338+26del
XM_011540619.1:c.1686+25_1686+26del	XP_011538921.1:n.1686+25_1686+26del
XM_011540621.1:c.1194+25_1194+26del	XP_011538923.1:n.1194+25_1194+26del
NM_000085.5:c.1845+25_1845+26del MANE Select	NP_000076.2:n.1845+25_1845+26del