Canonical Allele Identifier: CA2479314210

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804109_150804110delinsCA , CM000663.2:g.150804109_150804110delinsCA	GRCh38
NC_000001.10:g.150776585_150776586delinsCA , CM000663.1:g.150776585_150776586delinsCA	GRCh37
NC_000001.9:g.149043209_149043210delinsCA	NCBI36
NG_011848.1:g.9227_9228delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.529_530delinsTG MANE Select	ENSP00000271651.3:p.Cys177=
ENST00000443913.2:c.706_707delinsTG	ENSP00000405083.2:p.Cys236=
ENST00000480670.2:n.3598_3599delinsTG
ENST00000676680.1:c.529_530delinsTG	ENSP00000503270.1:p.Cys177=
ENST00000676716.1:c.406_407delinsTG	ENSP00000504737.1:p.Cys136=
ENST00000676751.1:c.529_530delinsTG	ENSP00000502964.1:p.Cys177=
ENST00000676824.1:c.529_530delinsTG	ENSP00000504176.1:p.Cys177=
ENST00000676966.1:c.529_530delinsTG	ENSP00000503723.1:p.Cys177=
ENST00000676970.1:c.529_530delinsTG	ENSP00000503832.1:p.Cys177=
ENST00000677330.1:n.2355_2356delinsTG
ENST00000677611.1:n.381_382delinsTG
ENST00000677887.1:c.571_572delinsTG	ENSP00000503876.1:p.Cys191=
ENST00000678275.1:c.*421_*422delinsTG	ENSP00000504796.1:n.*421_*422delinsTG
ENST00000678337.1:c.565_566delinsTG	ENSP00000504759.1:p.Cys189=
ENST00000678725.1:n.1506_1507delinsTG
ENST00000679090.1:n.1114_1115delinsTG
ENST00000679148.1:n.3491_3492delinsTG
ENST00000679171.1:n.2890_2891delinsTG
ENST00000679260.1:c.399+1751_399+1752delinsTG	ENSP00000504534.1:n.399+1751_399+1752delinsTG
ENST00000271651.7:c.529_530delinsTG	ENSP00000271651.3:p.Cys177=
ENST00000443913.1:c.706_707delinsTG	ENSP00000405083.1:p.Cys236=
ENST00000480670.1:n.369_370delinsTG
NM_000396.3:c.529_530delinsTG	NP_000387.1:p.Cys177=
NM_000396.4:c.529_530delinsTG MANE Select	NP_000387.1:p.Cys177=