Canonical Allele Identifier: CA2479314221

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804149G= , CM000663.2:g.150804149G=	GRCh38
NC_000001.10:g.150776625G= , CM000663.1:g.150776625G=	GRCh37
NC_000001.9:g.149043249G=	NCBI36
NG_011848.1:g.9188C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.490C= MANE Select	ENSP00000271651.3:p.Pro164=
ENST00000443913.2:c.667C=	ENSP00000405083.2:p.Pro223=
ENST00000480670.2:n.3559C=
ENST00000676680.1:c.490C=	ENSP00000503270.1:p.Pro164=
ENST00000676716.1:c.367C=	ENSP00000504737.1:p.Pro123=
ENST00000676751.1:c.490C=	ENSP00000502964.1:p.Pro164=
ENST00000676824.1:c.490C=	ENSP00000504176.1:p.Pro164=
ENST00000676966.1:c.490C=	ENSP00000503723.1:p.Pro164=
ENST00000676970.1:c.490C=	ENSP00000503832.1:p.Pro164=
ENST00000677330.1:n.2316C=
ENST00000677611.1:n.342C=
ENST00000677887.1:c.532C=	ENSP00000503876.1:p.Pro178=
ENST00000678275.1:c.*382C=	ENSP00000504796.1:n.*382C=
ENST00000678337.1:c.526C=	ENSP00000504759.1:p.Pro176=
ENST00000678725.1:n.1467C=
ENST00000679090.1:n.1075C=
ENST00000679148.1:n.3452C=
ENST00000679171.1:n.2851C=
ENST00000679260.1:c.399+1712C=	ENSP00000504534.1:n.399+1712C=
ENST00000271651.7:c.490C=	ENSP00000271651.3:p.Pro164=
ENST00000443913.1:c.667C=	ENSP00000405083.1:p.Pro223=
ENST00000480670.1:n.330C=
NM_000396.3:c.490C=	NP_000387.1:p.Pro164=
NM_000396.4:c.490C= MANE Select	NP_000387.1:p.Pro164=