Canonical Allele Identifier: CA1140886773

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796799T= , CM000663.2:g.150796799T=	GRCh38
NC_000001.10:g.150769275T= , CM000663.1:g.150769275T=	GRCh37
NC_000001.9:g.149035899T=	NCBI36
NG_011848.1:g.16538A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.990A= MANE Select	ENSP00000271651.3:p.Ter330=
ENST00000443913.2:c.1167A=	ENSP00000405083.2:p.Ter389=
ENST00000480670.2:n.4059A=
ENST00000676680.1:c.*284A=	ENSP00000503270.1:n.*284A=
ENST00000676716.1:c.867A=	ENSP00000504737.1:p.Ter289=
ENST00000676751.1:c.884A=	ENSP00000502964.1:p.Asp295=
ENST00000676824.1:c.990A=	ENSP00000504176.1:p.Ter330=
ENST00000676966.1:c.990A=	ENSP00000503723.1:p.Ter330=
ENST00000676970.1:c.1002A=	ENSP00000503832.1:p.Ter334=
ENST00000677330.1:n.2816A=
ENST00000677611.1:n.842A=
ENST00000677887.1:c.1032A=	ENSP00000503876.1:p.Ter344=
ENST00000678275.1:c.*882A=	ENSP00000504796.1:n.*882A=
ENST00000678337.1:c.1026A=	ENSP00000504759.1:p.Ter342=
ENST00000678725.1:n.2237A=
ENST00000679090.1:n.1845A=
ENST00000679148.1:n.3952A=
ENST00000679171.1:n.3621A=
ENST00000679178.1:n.701A=
ENST00000679260.1:c.771A=	ENSP00000504534.1:p.Ter257=
ENST00000271651.7:c.990A=	ENSP00000271651.3:p.Ter330=
NM_000396.3:c.990A=	NP_000387.1:p.Ter330=
NM_000396.4:c.990A= MANE Select	NP_000387.1:p.Ter330=