Canonical Allele Identifier: CA2643560172
Gene: CLCNKA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16024950del , CM000663.2:g.16024950del GRCh38
NC_000001.10:g.16351445del , CM000663.1:g.16351445del GRCh37
NC_000001.9:g.16224032del NCBI36
NG_009359.1:g.7960del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331433.5:c.358+59del MANE Select ENSP00000332771.4:n.358+59del
ENST00000331433.4:c.358+59del ENSP00000332771.4:n.358+59del
ENST00000375692.5:c.358+59del ENSP00000364844.1:n.358+59del
ENST00000439316.6:c.229+1022del ENSP00000414445.2:n.229+1022del
ENST00000464764.5:n.921+59del
ENST00000495784.1:n.516+59del
NM_001042704.1:c.358+59del NP_001036169.1:n.358+59del
NM_001257139.1:c.229+1022del NP_001244068.1:n.229+1022del
NM_004070.3:c.358+59del NP_004061.3:n.358+59del
NM_004070.4:c.358+59del MANE Select NP_004061.3:n.358+59del
NM_001042704.2:c.358+59del NP_001036169.1:n.358+59del
NM_001257139.2:c.229+1022del NP_001244068.1:n.229+1022del