Canonical Allele Identifier: CA2643564979

Gene: CLCNKB

Linked Data

• gnomAD v4: 1-16055511-TCCTGGACACCAGGTGGGTACTCCTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055512_16055537del , CM000663.2:g.16055512_16055537del	GRCh38
NC_000001.10:g.16382007_16382032del , CM000663.1:g.16382007_16382032del	GRCh37
NC_000001.9:g.16254594_16254619del	NCBI36
NG_013079.1:g.16761_16786del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1834_1845+14del
ENST00000682793.1:c.1834_1845+14del
ENST00000682838.1:c.*1576_*1587+14del
ENST00000683578.1:c.1834_1845+14del
ENST00000683606.1:n.1440_1451+14del
ENST00000683661.1:n.3369_3380+14del
ENST00000684324.1:c.1834_1845+14del
ENST00000684545.1:c.1834_1845+14del
ENST00000684624.1:n.1211_1222+14del
ENST00000684714.1:c.*54_*65+14del
ENST00000684731.1:n.1161_1172+14del
ENST00000375679.9:c.1834_1845+14del
ENST00000375667.7:c.1327_1338+14del
ENST00000375679.8:c.1834_1845+14del
ENST00000431772.1:c.301_312+14del
ENST00000619181.4:c.1294-1675_1294-1650del	ENSP00000483866.1:n.1294-1675_1294-1650del
NM_000085.4:c.1834_1845+14del
NM_001165945.2:c.1327_1338+14del
XM_011540619.1:c.1675_1686+14del
XM_011540621.1:c.1183_1194+14del
NM_000085.5:c.1834_1845+14del