Canonical Allele Identifier: CA2479314194

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804061_150804063delinsCGG , CM000663.2:g.150804061_150804063delinsCGG	GRCh38
NC_000001.10:g.150776537_150776539delinsCGG , CM000663.1:g.150776537_150776539delinsCGG	GRCh37
NC_000001.9:g.149043161_149043163delinsCGG	NCBI36
NG_011848.1:g.9274_9276delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.576_578delinsCCG MANE Select	ENSP00000271651.3:p.Asn192=
ENST00000443913.2:c.753_755delinsCCG	ENSP00000405083.2:p.Asn251=
ENST00000480670.2:n.3645_3647delinsCCG
ENST00000676680.1:c.576_578delinsCCG	ENSP00000503270.1:p.Asn192=
ENST00000676716.1:c.453_455delinsCCG	ENSP00000504737.1:p.Asn151=
ENST00000676751.1:c.576_578delinsCCG	ENSP00000502964.1:p.Asn192=
ENST00000676824.1:c.576_578delinsCCG	ENSP00000504176.1:p.Asn192=
ENST00000676966.1:c.576_578delinsCCG	ENSP00000503723.1:p.Asn192=
ENST00000676970.1:c.576_578delinsCCG	ENSP00000503832.1:p.Asn192=
ENST00000677330.1:n.2402_2404delinsCCG
ENST00000677611.1:n.428_430delinsCCG
ENST00000677887.1:c.618_620delinsCCG	ENSP00000503876.1:p.Asn206=
ENST00000678275.1:c.*468_*470delinsCCG	ENSP00000504796.1:n.*468_*470delinsCCG
ENST00000678337.1:c.612_614delinsCCG	ENSP00000504759.1:p.Asn204=
ENST00000678725.1:n.1553_1555delinsCCG
ENST00000679090.1:n.1161_1163delinsCCG
ENST00000679148.1:n.3538_3540delinsCCG
ENST00000679171.1:n.2937_2939delinsCCG
ENST00000679260.1:c.399+1798_399+1800delinsCCG	ENSP00000504534.1:n.399+1798_399+1800delinsCCG
ENST00000271651.7:c.576_578delinsCCG	ENSP00000271651.3:p.Asn192=
ENST00000443913.1:c.753_755delinsCCG	ENSP00000405083.1:p.Asn251=
ENST00000480670.1:n.416_418delinsCCG
NM_000396.3:c.576_578delinsCCG	NP_000387.1:p.Asn192=
NM_000396.4:c.576_578delinsCCG MANE Select	NP_000387.1:p.Asn192=