Canonical Allele Identifier: CA2643565624

Gene: CLCNKB

Linked Data

• gnomAD v4: 1-16055574-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055575_16055576del , CM000663.2:g.16055575_16055576del	GRCh38
NC_000001.10:g.16382070_16382071del , CM000663.1:g.16382070_16382071del	GRCh37
NC_000001.9:g.16254657_16254658del	NCBI36
NG_013079.1:g.16824_16825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1845+52_1845+53del	ENSP00000507062.1:n.1845+52_1845+53del
ENST00000682793.1:c.1845+52_1845+53del	ENSP00000506910.1:n.1845+52_1845+53del
ENST00000682838.1:c.*1587+52_*1587+53del	ENSP00000507652.1:n.*1587+52_*1587+53del
ENST00000683578.1:c.1845+52_1845+53del	ENSP00000507430.1:n.1845+52_1845+53del
ENST00000683606.1:n.1451+52_1451+53del
ENST00000683661.1:n.3380+52_3380+53del
ENST00000684324.1:c.1845+52_1845+53del	ENSP00000507937.1:n.1845+52_1845+53del
ENST00000684545.1:c.1845+52_1845+53del	ENSP00000506733.1:n.1845+52_1845+53del
ENST00000684624.1:n.1222+52_1222+53del
ENST00000684714.1:c.*65+52_*65+53del	ENSP00000506861.1:n.*65+52_*65+53del
ENST00000684731.1:n.1172+52_1172+53del
ENST00000375679.9:c.1845+52_1845+53del MANE Select	ENSP00000364831.5:n.1845+52_1845+53del
ENST00000375667.7:c.1338+52_1338+53del	ENSP00000364819.3:n.1338+52_1338+53del
ENST00000375679.8:c.1845+52_1845+53del	ENSP00000364831.4:n.1845+52_1845+53del
ENST00000431772.1:c.312+52_312+53del	ENSP00000389344.1:n.312+52_312+53del
ENST00000619181.4:c.1294-1612_1294-1611del	ENSP00000483866.1:n.1294-1612_1294-1611del
NM_000085.4:c.1845+52_1845+53del	NP_000076.2:n.1845+52_1845+53del
NM_001165945.2:c.1338+52_1338+53del	NP_001159417.2:n.1338+52_1338+53del
XM_011540619.1:c.1686+52_1686+53del	XP_011538921.1:n.1686+52_1686+53del
XM_011540621.1:c.1194+52_1194+53del	XP_011538923.1:n.1194+52_1194+53del
NM_000085.5:c.1845+52_1845+53del MANE Select	NP_000076.2:n.1845+52_1845+53del