Canonical Allele Identifier: CA1143359297

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804023G= , CM000663.2:g.150804023G=	GRCh38
NC_000001.10:g.150776499G= , CM000663.1:g.150776499G=	GRCh37
NC_000001.9:g.149043123G=	NCBI36
NG_011848.1:g.9314C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.616C= MANE Select	ENSP00000271651.3:p.Gln206=
ENST00000443913.2:c.793C=	ENSP00000405083.2:p.Gln265=
ENST00000480670.2:n.3685C=
ENST00000676680.1:c.616C=	ENSP00000503270.1:p.Gln206=
ENST00000676716.1:c.493C=	ENSP00000504737.1:p.Gln165=
ENST00000676751.1:c.616C=	ENSP00000502964.1:p.Gln206=
ENST00000676824.1:c.616C=	ENSP00000504176.1:p.Gln206=
ENST00000676966.1:c.616C=	ENSP00000503723.1:p.Gln206=
ENST00000676970.1:c.616C=	ENSP00000503832.1:p.Gln206=
ENST00000677330.1:n.2442C=
ENST00000677611.1:n.468C=
ENST00000677887.1:c.658C=	ENSP00000503876.1:p.Gln220=
ENST00000678275.1:c.*508C=	ENSP00000504796.1:n.*508C=
ENST00000678337.1:c.652C=	ENSP00000504759.1:p.Gln218=
ENST00000678725.1:n.1593C=
ENST00000679090.1:n.1201C=
ENST00000679148.1:n.3578C=
ENST00000679171.1:n.2977C=
ENST00000679260.1:c.399+1838C=	ENSP00000504534.1:n.399+1838C=
ENST00000271651.7:c.616C=	ENSP00000271651.3:p.Gln206=
ENST00000480670.1:n.456C=
NM_000396.3:c.616C=	NP_000387.1:p.Gln206=
NM_000396.4:c.616C= MANE Select	NP_000387.1:p.Gln206=