Canonical Allele Identifier: CA2573895739
Gene: CTSS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150733143del , CM000663.2:g.150733143del GRCh38
NC_000001.10:g.150705619del , CM000663.1:g.150705619del GRCh37
NC_000001.9:g.148972243del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368985.8:c.902del MANE Select ENSP00000357981.3:p.Gly301AlafsTer?
ENST00000448301.7:c.674del ENSP00000408414.2:p.Gly225AlafsTer?
ENST00000472977.7:c.902del ENSP00000475176.2:p.Gly301AlafsTer?
ENST00000483930.2:c.*96del ENSP00000475812.2:n.*96del
ENST00000607427.2:c.902del ENSP00000475557.2:p.Gly301AlafsTer?
ENST00000679512.1:c.799del ENSP00000505113.1:p.Ala267ProfsTer5
ENST00000679898.1:c.629del ENSP00000505326.1:p.Gly210AlafsTer?
ENST00000680288.1:c.752del ENSP00000506001.1:p.Gly251AlafsTer?
ENST00000680311.1:c.633del ENSP00000505020.1:p.Pro212HisfsTer?
ENST00000680471.1:c.*73del ENSP00000506603.1:n.*73del
ENST00000680664.1:c.725del ENSP00000506248.1:p.Gly242AlafsTer?
ENST00000680931.1:c.*252del ENSP00000504934.1:n.*252del
ENST00000681357.1:n.292del
ENST00000681444.1:c.902del ENSP00000505359.1:p.Gly301AlafsTer?
ENST00000368985.7:c.902del ENSP00000357981.3:p.Gly301AlafsTer?
ENST00000448301.6:c.752del ENSP00000408414.1:p.Gly251AlafsTer?
ENST00000472977.6:c.195del
ENST00000483930.1:c.450del ENSP00000475812.1:n.450del
NM_001199739.1:c.752del NP_001186668.1:p.Gly251AlafsTer?
NM_004079.4:c.902del NP_004070.3:p.Gly301AlafsTer?
NM_004079.5:c.902del MANE Select NP_004070.3:p.Gly301AlafsTer?
NM_001199739.2:c.752del NP_001186668.1:p.Gly251AlafsTer?