Canonical Allele Identifier: CA2479314232

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804188_150804216delinsGGCCCTCCAGGGCACCCACAGAGCTAAAA , CM000663.2:g.150804188_150804216delinsGGCCCTCCAGGGCACCCACAGAGCTAAAA	GRCh38
NC_000001.10:g.150776664_150776692delinsGGCCCTCCAGGGCACCCACAGAGCTAAAA , CM000663.1:g.150776664_150776692delinsGGCCCTCCAGGGCACCCACAGAGCTAAAA	GRCh37
NC_000001.9:g.149043288_149043316delinsGGCCCTCCAGGGCACCCACAGAGCTAAAA	NCBI36
NG_011848.1:g.9121_9149delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC MANE Select	ENSP00000271651.3:p.Ala141=
ENST00000443913.2:c.600_628delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000405083.2:p.Ala200=
ENST00000480670.2:n.3492_3520delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
ENST00000676680.1:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000503270.1:p.Ala141=
ENST00000676716.1:c.300_328delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000504737.1:p.Ala100=
ENST00000676751.1:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000502964.1:p.Ala141=
ENST00000676824.1:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000504176.1:p.Ala141=
ENST00000676966.1:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000503723.1:p.Ala141=
ENST00000676970.1:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000503832.1:p.Ala141=
ENST00000677330.1:n.2249_2277delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
ENST00000677611.1:n.275_303delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
ENST00000677887.1:c.465_493delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000503876.1:p.Ala155=
ENST00000678275.1:c.*315_*343delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000504796.1:n.*315_*343delinsTTTTAG...
ENST00000678337.1:c.459_487delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000504759.1:p.Ala153=
ENST00000678725.1:n.1400_1428delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
ENST00000679090.1:n.1008_1036delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
ENST00000679148.1:n.3385_3413delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
ENST00000679171.1:n.2784_2812delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
ENST00000679260.1:c.399+1645_399+1673delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000504534.1:n.399+1645_399+1673deli...
ENST00000271651.7:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000271651.3:p.Ala141=
ENST00000443913.1:c.600_628delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	ENSP00000405083.1:p.Ala200=
ENST00000480670.1:n.263_291delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC
NM_000396.3:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC	NP_000387.1:p.Ala141=
NM_000396.4:c.423_451delinsTTTTAGCTCTGTGGGTGCCCTGGAGGGCC MANE Select	NP_000387.1:p.Ala141=