Canonical Allele Identifier: CA1148571910

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804062G= , CM000663.2:g.150804062G=	GRCh38
NC_000001.10:g.150776538G= , CM000663.1:g.150776538G=	GRCh37
NC_000001.9:g.149043162G=	NCBI36
NG_011848.1:g.9275C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.577C= MANE Select	ENSP00000271651.3:p.Arg193=
ENST00000443913.2:c.754C=	ENSP00000405083.2:p.Arg252=
ENST00000480670.2:n.3646C=
ENST00000676680.1:c.577C=	ENSP00000503270.1:p.Arg193=
ENST00000676716.1:c.454C=	ENSP00000504737.1:p.Arg152=
ENST00000676751.1:c.577C=	ENSP00000502964.1:p.Arg193=
ENST00000676824.1:c.577C=	ENSP00000504176.1:p.Arg193=
ENST00000676966.1:c.577C=	ENSP00000503723.1:p.Arg193=
ENST00000676970.1:c.577C=	ENSP00000503832.1:p.Arg193=
ENST00000677330.1:n.2403C=
ENST00000677611.1:n.429C=
ENST00000677887.1:c.619C=	ENSP00000503876.1:p.Arg207=
ENST00000678275.1:c.*469C=	ENSP00000504796.1:n.*469C=
ENST00000678337.1:c.613C=	ENSP00000504759.1:p.Arg205=
ENST00000678725.1:n.1554C=
ENST00000679090.1:n.1162C=
ENST00000679148.1:n.3539C=
ENST00000679171.1:n.2938C=
ENST00000679260.1:c.399+1799C=	ENSP00000504534.1:n.399+1799C=
ENST00000271651.7:c.577C=	ENSP00000271651.3:p.Arg193=
ENST00000443913.1:c.754C=	ENSP00000405083.1:p.Arg252=
ENST00000480670.1:n.417C=
NM_000396.3:c.577C=	NP_000387.1:p.Arg193=
NM_000396.4:c.577C= MANE Select	NP_000387.1:p.Arg193=