Canonical Allele Identifier: CA2479314154

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150803953_150803974delinsCAGTACAAAACATCATGCTGGG , CM000663.2:g.150803953_150803974delinsCAGTACAAAACATCATGCTGGG	GRCh38
NC_000001.10:g.150776429_150776450delinsCAGTACAAAACATCATGCTGGG , CM000663.1:g.150776429_150776450delinsCAGTACAAAACATCATGCTGGG	GRCh37
NC_000001.9:g.149043053_149043074delinsCAGTACAAAACATCATGCTGGG	NCBI36
NG_011848.1:g.9363_9384delinsCCCAGCATGATGTTTTGTACTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG MANE Select	ENSP00000271651.3:n.618+47_618+68delinsCC...
ENST00000443913.2:c.795+47_795+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000405083.2:n.795+47_795+68delinsCC...
ENST00000480670.2:n.3687+47_3687+68delinsCCCAGCATGATGTTTTGTACTG
ENST00000676680.1:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000503270.1:n.618+47_618+68delinsCC...
ENST00000676716.1:c.495+47_495+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000504737.1:n.495+47_495+68delinsCC...
ENST00000676751.1:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000502964.1:n.618+47_618+68delinsCC...
ENST00000676824.1:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000504176.1:n.618+47_618+68delinsCC...
ENST00000676966.1:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000503723.1:n.618+47_618+68delinsCC...
ENST00000676970.1:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000503832.1:n.618+47_618+68delinsCC...
ENST00000677330.1:n.2444+47_2444+68delinsCCCAGCATGATGTTTTGTACTG
ENST00000677611.1:n.470+47_470+68delinsCCCAGCATGATGTTTTGTACTG
ENST00000677887.1:c.660+47_660+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000503876.1:n.660+47_660+68delinsCC...
ENST00000678275.1:c.*510+47_*510+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000504796.1:n.*510+47_*510+68delins...
ENST00000678337.1:c.654+47_654+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000504759.1:n.654+47_654+68delinsCC...
ENST00000678725.1:n.1595+47_1595+68delinsCCCAGCATGATGTTTTGTACTG
ENST00000679090.1:n.1203+47_1203+68delinsCCCAGCATGATGTTTTGTACTG
ENST00000679148.1:n.3580+47_3580+68delinsCCCAGCATGATGTTTTGTACTG
ENST00000679171.1:n.2979+47_2979+68delinsCCCAGCATGATGTTTTGTACTG
ENST00000679260.1:c.399+1887_399+1908delinsCCCAGCATGATGTTTTGTACTG	ENSP00000504534.1:n.399+1887_399+1908deli...
ENST00000271651.7:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG	ENSP00000271651.3:n.618+47_618+68delinsCC...
NM_000396.3:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG	NP_000387.1:n.618+47_618+68delinsCCCAGCAT...
NM_000396.4:c.618+47_618+68delinsCCCAGCATGATGTTTTGTACTG MANE Select	NP_000387.1:n.618+47_618+68delinsCCCAGCAT...