Canonical Allele Identifier: CA1140886775

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799607G= , CM000663.2:g.150799607G=	GRCh38
NC_000001.10:g.150772083G= , CM000663.1:g.150772083G=	GRCh37
NC_000001.9:g.149038707G=	NCBI36
NG_011848.1:g.13730C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.721C= MANE Select	ENSP00000271651.3:p.Arg241=
ENST00000443913.2:c.898C=	ENSP00000405083.2:p.Arg300=
ENST00000480670.2:n.3790C=
ENST00000676680.1:c.*15C=	ENSP00000503270.1:n.*15C=
ENST00000676716.1:c.598C=	ENSP00000504737.1:p.Arg200=
ENST00000676751.1:c.721C=	ENSP00000502964.1:p.Arg241=
ENST00000676824.1:c.721C=	ENSP00000504176.1:p.Arg241=
ENST00000676966.1:c.721C=	ENSP00000503723.1:p.Arg241=
ENST00000676970.1:c.721C=	ENSP00000503832.1:p.Arg241=
ENST00000677330.1:n.2547C=
ENST00000677611.1:n.573C=
ENST00000677887.1:c.763C=	ENSP00000503876.1:p.Arg255=
ENST00000678275.1:c.*613C=	ENSP00000504796.1:n.*613C=
ENST00000678337.1:c.757C=	ENSP00000504759.1:p.Arg253=
ENST00000678725.1:n.1698C=
ENST00000679090.1:n.1306C=
ENST00000679148.1:n.3683C=
ENST00000679171.1:n.3082C=
ENST00000679178.1:n.432C=
ENST00000679260.1:c.502C=	ENSP00000504534.1:p.Arg168=
ENST00000271651.7:c.721C=	ENSP00000271651.3:p.Arg241=
NM_000396.3:c.721C=	NP_000387.1:p.Arg241=
NM_000396.4:c.721C= MANE Select	NP_000387.1:p.Arg241=