Canonical Allele Identifier: CA2643565375
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16055550_16055551insTGGGGGTG , CM000663.2:g.16055550_16055551insTGGGGGTG GRCh38
NC_000001.10:g.16382045_16382046insTGGGGGTG , CM000663.1:g.16382045_16382046insTGGGGGTG GRCh37
NC_000001.9:g.16254632_16254633insTGGGGGTG NCBI36
NG_013079.1:g.16799_16800insTGGGGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1845+27_1845+28insTGGGGGTG ENSP00000507062.1:n.1845+27_1845+28insTGGGGGTG
ENST00000682793.1:c.1845+27_1845+28insTGGGGGTG ENSP00000506910.1:n.1845+27_1845+28insTGGGGGTG
ENST00000682838.1:c.*1587+27_*1587+28insTGGGGGTG ENSP00000507652.1:n.*1587+27_*1587+28insTGGGGGTG
ENST00000683578.1:c.1845+27_1845+28insTGGGGGTG ENSP00000507430.1:n.1845+27_1845+28insTGGGGGTG
ENST00000683606.1:n.1451+27_1451+28insTGGGGGTG
ENST00000683661.1:n.3380+27_3380+28insTGGGGGTG
ENST00000684324.1:c.1845+27_1845+28insTGGGGGTG ENSP00000507937.1:n.1845+27_1845+28insTGGGGGTG
ENST00000684545.1:c.1845+27_1845+28insTGGGGGTG ENSP00000506733.1:n.1845+27_1845+28insTGGGGGTG
ENST00000684624.1:n.1222+27_1222+28insTGGGGGTG
ENST00000684714.1:c.*65+27_*65+28insTGGGGGTG ENSP00000506861.1:n.*65+27_*65+28insTGGGGGTG
ENST00000684731.1:n.1172+27_1172+28insTGGGGGTG
ENST00000375679.9:c.1845+27_1845+28insTGGGGGTG MANE Select ENSP00000364831.5:n.1845+27_1845+28insTGGGGGTG
ENST00000375667.7:c.1338+27_1338+28insTGGGGGTG ENSP00000364819.3:n.1338+27_1338+28insTGGGGGTG
ENST00000375679.8:c.1845+27_1845+28insTGGGGGTG ENSP00000364831.4:n.1845+27_1845+28insTGGGGGTG
ENST00000431772.1:c.312+27_312+28insTGGGGGTG ENSP00000389344.1:n.312+27_312+28insTGGGGGTG
ENST00000619181.4:c.1294-1637_1294-1636insTGGGGGTG ENSP00000483866.1:n.1294-1637_1294-1636insTGGGGGTG
NM_000085.4:c.1845+27_1845+28insTGGGGGTG NP_000076.2:n.1845+27_1845+28insTGGGGGTG
NM_001165945.2:c.1338+27_1338+28insTGGGGGTG NP_001159417.2:n.1338+27_1338+28insTGGGGGTG
XM_011540619.1:c.1686+27_1686+28insTGGGGGTG XP_011538921.1:n.1686+27_1686+28insTGGGGGTG
XM_011540621.1:c.1194+27_1194+28insTGGGGGTG XP_011538923.1:n.1194+27_1194+28insTGGGGGTG
NM_000085.5:c.1845+27_1845+28insTGGGGGTG MANE Select NP_000076.2:n.1845+27_1845+28insTGGGGGTG