Canonical Allele Identifier: CA2586967419
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804189_150804211del , CM000663.2:g.150804189_150804211del GRCh38
NC_000001.10:g.150776665_150776687del , CM000663.1:g.150776665_150776687del GRCh37
NC_000001.9:g.149043289_149043311del NCBI36
NG_011848.1:g.9126_9148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.428_450del MANE Select ENSP00000271651.3:p.Ser143ThrfsTer23
ENST00000443913.2:c.605_627del ENSP00000405083.2:p.Ser202ThrfsTer23
ENST00000480670.2:n.3497_3519del
ENST00000676680.1:c.428_450del ENSP00000503270.1:p.Ser143ThrfsTer23
ENST00000676716.1:c.305_327del ENSP00000504737.1:p.Ser102ThrfsTer23
ENST00000676751.1:c.428_450del ENSP00000502964.1:p.Ser143ThrfsTer23
ENST00000676824.1:c.428_450del ENSP00000504176.1:p.Ser143ThrfsTer23
ENST00000676966.1:c.428_450del ENSP00000503723.1:p.Ser143ThrfsTer23
ENST00000676970.1:c.428_450del ENSP00000503832.1:p.Ser143ThrfsTer23
ENST00000677330.1:n.2254_2276del
ENST00000677611.1:n.280_302del
ENST00000677887.1:c.470_492del ENSP00000503876.1:p.Ser157ThrfsTer23
ENST00000678275.1:c.*320_*342del ENSP00000504796.1:n.*320_*342del
ENST00000678337.1:c.464_486del ENSP00000504759.1:p.Ser155ThrfsTer23
ENST00000678725.1:n.1405_1427del
ENST00000679090.1:n.1013_1035del
ENST00000679148.1:n.3390_3412del
ENST00000679171.1:n.2789_2811del
ENST00000679260.1:c.399+1650_399+1672del ENSP00000504534.1:n.399+1650_399+1672del
ENST00000271651.7:c.428_450del ENSP00000271651.3:p.Ser143ThrfsTer23
ENST00000443913.1:c.605_627del ENSP00000405083.1:p.Ser202ThrfsTer23
ENST00000480670.1:n.268_290del
NM_000396.3:c.428_450del NP_000387.1:p.Ser143ThrfsTer23
NM_000396.4:c.428_450del MANE Select NP_000387.1:p.Ser143ThrfsTer23