Canonical Allele Identifier: CA2643562731
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16048235_16048236insCCTGGGAGATGGG , CM000663.2:g.16048235_16048236insCCTGGGAGATGGG GRCh38
NC_000001.10:g.16374730_16374731insCCTGGGAGATGGG , CM000663.1:g.16374730_16374731insCCTGGGAGATGGG GRCh37
NC_000001.9:g.16247317_16247318insCCTGGGAGATGGG NCBI36
NG_013079.1:g.9484_9485insCCTGGGAGATGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.499-108_499-107insCCTGGGAGATGGG ENSP00000507062.1:n.499-108_499-107insCCTGGGAGATGGG
ENST00000682793.1:c.499-108_499-107insCCTGGGAGATGGG ENSP00000506910.1:n.499-108_499-107insCCTGGGAGATGGG
ENST00000682838.1:c.*157-108_*157-107insCCTGGGAGATGGG ENSP00000507652.1:n.*157-108_*157-107insCCTGGGAGATGGG
ENST00000683578.1:c.499-108_499-107insCCTGGGAGATGGG ENSP00000507430.1:n.499-108_499-107insCCTGGGAGATGGG
ENST00000683661.1:n.2034-108_2034-107insCCTGGGAGATGGG
ENST00000684324.1:c.499-108_499-107insCCTGGGAGATGGG ENSP00000507937.1:n.499-108_499-107insCCTGGGAGATGGG
ENST00000684545.1:c.499-108_499-107insCCTGGGAGATGGG ENSP00000506733.1:n.499-108_499-107insCCTGGGAGATGGG
ENST00000684714.1:c.499-108_499-107insCCTGGGAGATGGG ENSP00000506861.1:n.499-108_499-107insCCTGGGAGATGGG
ENST00000375679.9:c.499-108_499-107insCCTGGGAGATGGG MANE Select ENSP00000364831.5:n.499-108_499-107insCCTGGGAGATGGG
ENST00000375679.8:c.499-108_499-107insCCTGGGAGATGGG ENSP00000364831.4:n.499-108_499-107insCCTGGGAGATGGG
ENST00000619181.4:c.499-108_499-107insCCTGGGAGATGGG ENSP00000483866.1:n.499-108_499-107insCCTGGGAGATGGG
NM_000085.4:c.499-108_499-107insCCTGGGAGATGGG NP_000076.2:n.499-108_499-107insCCTGGGAGATGGG
XM_011540619.1:c.340-108_340-107insCCTGGGAGATGGG XP_011538921.1:n.340-108_340-107insCCTGGGAGATGGG
XM_011540620.1:c.499-108_499-107insCCTGGGAGATGGG XP_011538922.1:n.499-108_499-107insCCTGGGAGATGGG
NM_000085.5:c.499-108_499-107insCCTGGGAGATGGG MANE Select NP_000076.2:n.499-108_499-107insCCTGGGAGATGGG