Canonical Allele Identifier: CA2479314215

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804132A= , CM000663.2:g.150804132A=	GRCh38
NC_000001.10:g.150776608A= , CM000663.1:g.150776608A=	GRCh37
NC_000001.9:g.149043232A=	NCBI36
NG_011848.1:g.9205T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.507T= MANE Select	ENSP00000271651.3:p.Asp169=
ENST00000443913.2:c.684T=	ENSP00000405083.2:p.Asp228=
ENST00000480670.2:n.3576T=
ENST00000676680.1:c.507T=	ENSP00000503270.1:p.Asp169=
ENST00000676716.1:c.384T=	ENSP00000504737.1:p.Asp128=
ENST00000676751.1:c.507T=	ENSP00000502964.1:p.Asp169=
ENST00000676824.1:c.507T=	ENSP00000504176.1:p.Asp169=
ENST00000676966.1:c.507T=	ENSP00000503723.1:p.Asp169=
ENST00000676970.1:c.507T=	ENSP00000503832.1:p.Asp169=
ENST00000677330.1:n.2333T=
ENST00000677611.1:n.359T=
ENST00000677887.1:c.549T=	ENSP00000503876.1:p.Asp183=
ENST00000678275.1:c.*399T=	ENSP00000504796.1:n.*399T=
ENST00000678337.1:c.543T=	ENSP00000504759.1:p.Asp181=
ENST00000678725.1:n.1484T=
ENST00000679090.1:n.1092T=
ENST00000679148.1:n.3469T=
ENST00000679171.1:n.2868T=
ENST00000679260.1:c.399+1729T=	ENSP00000504534.1:n.399+1729T=
ENST00000271651.7:c.507T=	ENSP00000271651.3:p.Asp169=
ENST00000443913.1:c.684T=	ENSP00000405083.1:p.Asp228=
ENST00000480670.1:n.347T=
NM_000396.3:c.507T=	NP_000387.1:p.Asp169=
NM_000396.4:c.507T= MANE Select	NP_000387.1:p.Asp169=