Canonical Allele Identifier: CA645534129
Gene: CTSK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804104del , CM000663.2:g.150804104del GRCh38
NC_000001.10:g.150776580del , CM000663.1:g.150776580del GRCh37
NC_000001.9:g.149043204del NCBI36
NG_011848.1:g.9237del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.539del MANE Select ENSP00000271651.3:p.Gly180AlafsTer3
ENST00000443913.2:c.716del ENSP00000405083.2:p.Gly239AlafsTer3
ENST00000480670.2:n.3608del
ENST00000676680.1:c.539del ENSP00000503270.1:p.Gly180AlafsTer3
ENST00000676716.1:c.416del ENSP00000504737.1:p.Gly139AlafsTer3
ENST00000676751.1:c.539del ENSP00000502964.1:p.Gly180AlafsTer3
ENST00000676824.1:c.539del ENSP00000504176.1:p.Gly180AlafsTer3
ENST00000676966.1:c.539del ENSP00000503723.1:p.Gly180AlafsTer3
ENST00000676970.1:c.539del ENSP00000503832.1:p.Gly180AlafsTer3
ENST00000677330.1:n.2365del
ENST00000677611.1:n.391del
ENST00000677887.1:c.581del ENSP00000503876.1:p.Gly194AlafsTer3
ENST00000678275.1:c.*431del ENSP00000504796.1:n.*431del
ENST00000678337.1:c.575del ENSP00000504759.1:p.Gly192AlafsTer3
ENST00000678725.1:n.1516del
ENST00000679090.1:n.1124del
ENST00000679148.1:n.3501del
ENST00000679171.1:n.2900del
ENST00000679260.1:c.399+1761del ENSP00000504534.1:n.399+1761del
ENST00000271651.7:c.539del ENSP00000271651.3:p.Gly180AlafsTer3
ENST00000443913.1:c.716del ENSP00000405083.1:p.Gly239AlafsTer3
ENST00000480670.1:n.379del
NM_000396.3:c.539del NP_000387.1:p.Gly180AlafsTer3
NM_000396.4:c.539del MANE Select NP_000387.1:p.Gly180AlafsTer3