Canonical Allele Identifier: CA2643560019
Gene: CLCNKA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16024667del , CM000663.2:g.16024667del GRCh38
NC_000001.10:g.16351162del , CM000663.1:g.16351162del GRCh37
NC_000001.9:g.16223749del NCBI36
NG_009359.1:g.7677del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331433.5:c.230-96del MANE Select ENSP00000332771.4:n.230-96del
ENST00000331433.4:c.230-96del ENSP00000332771.4:n.230-96del
ENST00000375692.5:c.230-96del ENSP00000364844.1:n.230-96del
ENST00000439316.6:c.229+739del ENSP00000414445.2:n.229+739del
ENST00000464764.5:n.889-192del
ENST00000495784.1:n.388-96del
NM_001042704.1:c.230-96del NP_001036169.1:n.230-96del
NM_001257139.1:c.229+739del NP_001244068.1:n.229+739del
NM_004070.3:c.230-96del NP_004061.3:n.230-96del
NM_004070.4:c.230-96del MANE Select NP_004061.3:n.230-96del
NM_001042704.2:c.230-96del NP_001036169.1:n.230-96del
NM_001257139.2:c.229+739del NP_001244068.1:n.229+739del