Canonical Allele Identifier: CA2574054760

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150803975del , CM000663.2:g.150803975del	GRCh38
NC_000001.10:g.150776451del , CM000663.1:g.150776451del	GRCh37
NC_000001.9:g.149043075del	NCBI36
NG_011848.1:g.9365del

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.618+49del MANE Select	ENSP00000271651.3:n.618+49del
ENST00000443913.2:c.795+49del	ENSP00000405083.2:n.795+49del
ENST00000480670.2:n.3687+49del
ENST00000676680.1:c.618+49del	ENSP00000503270.1:n.618+49del
ENST00000676716.1:c.495+49del	ENSP00000504737.1:n.495+49del
ENST00000676751.1:c.618+49del	ENSP00000502964.1:n.618+49del
ENST00000676824.1:c.618+49del	ENSP00000504176.1:n.618+49del
ENST00000676966.1:c.618+49del	ENSP00000503723.1:n.618+49del
ENST00000676970.1:c.618+49del	ENSP00000503832.1:n.618+49del
ENST00000677330.1:n.2444+49del
ENST00000677611.1:n.470+49del
ENST00000677887.1:c.660+49del	ENSP00000503876.1:n.660+49del
ENST00000678275.1:c.*510+49del	ENSP00000504796.1:n.*510+49del
ENST00000678337.1:c.654+49del	ENSP00000504759.1:n.654+49del
ENST00000678725.1:n.1595+49del
ENST00000679090.1:n.1203+49del
ENST00000679148.1:n.3580+49del
ENST00000679171.1:n.2979+49del
ENST00000679260.1:c.399+1889del	ENSP00000504534.1:n.399+1889del
ENST00000271651.7:c.618+49del	ENSP00000271651.3:n.618+49del
NM_000396.3:c.618+49del	NP_000387.1:n.618+49del
NM_000396.4:c.618+49del MANE Select	NP_000387.1:n.618+49del