Canonical Allele Identifier: CA2643565139
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16055534_16055535insGGCG , CM000663.2:g.16055534_16055535insGGCG GRCh38
NC_000001.10:g.16382029_16382030insGGCG , CM000663.1:g.16382029_16382030insGGCG GRCh37
NC_000001.9:g.16254616_16254617insGGCG NCBI36
NG_013079.1:g.16783_16784insGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1845+11_1845+12insGGCG ENSP00000507062.1:n.1845+11_1845+12insGGCG
ENST00000682793.1:c.1845+11_1845+12insGGCG ENSP00000506910.1:n.1845+11_1845+12insGGCG
ENST00000682838.1:c.*1587+11_*1587+12insGGCG ENSP00000507652.1:n.*1587+11_*1587+12insGGCG
ENST00000683578.1:c.1845+11_1845+12insGGCG ENSP00000507430.1:n.1845+11_1845+12insGGCG
ENST00000683606.1:n.1451+11_1451+12insGGCG
ENST00000683661.1:n.3380+11_3380+12insGGCG
ENST00000684324.1:c.1845+11_1845+12insGGCG ENSP00000507937.1:n.1845+11_1845+12insGGCG
ENST00000684545.1:c.1845+11_1845+12insGGCG ENSP00000506733.1:n.1845+11_1845+12insGGCG
ENST00000684624.1:n.1222+11_1222+12insGGCG
ENST00000684714.1:c.*65+11_*65+12insGGCG ENSP00000506861.1:n.*65+11_*65+12insGGCG
ENST00000684731.1:n.1172+11_1172+12insGGCG
ENST00000375679.9:c.1845+11_1845+12insGGCG MANE Select ENSP00000364831.5:n.1845+11_1845+12insGGCG
ENST00000375667.7:c.1338+11_1338+12insGGCG ENSP00000364819.3:n.1338+11_1338+12insGGCG
ENST00000375679.8:c.1845+11_1845+12insGGCG ENSP00000364831.4:n.1845+11_1845+12insGGCG
ENST00000431772.1:c.312+11_312+12insGGCG ENSP00000389344.1:n.312+11_312+12insGGCG
ENST00000619181.4:c.1294-1653_1294-1652insGGCG ENSP00000483866.1:n.1294-1653_1294-1652insGGCG
NM_000085.4:c.1845+11_1845+12insGGCG NP_000076.2:n.1845+11_1845+12insGGCG
NM_001165945.2:c.1338+11_1338+12insGGCG NP_001159417.2:n.1338+11_1338+12insGGCG
XM_011540619.1:c.1686+11_1686+12insGGCG XP_011538921.1:n.1686+11_1686+12insGGCG
XM_011540621.1:c.1194+11_1194+12insGGCG XP_011538923.1:n.1194+11_1194+12insGGCG
NM_000085.5:c.1845+11_1845+12insGGCG MANE Select NP_000076.2:n.1845+11_1845+12insGGCG