Canonical Allele Identifier: CA1148422635

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804039G= , CM000663.2:g.150804039G=	GRCh38
NC_000001.10:g.150776515G= , CM000663.1:g.150776515G=	GRCh37
NC_000001.9:g.149043139G=	NCBI36
NG_011848.1:g.9298C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.600C= MANE Select	ENSP00000271651.3:p.Ala200=
ENST00000443913.2:c.777C=	ENSP00000405083.2:p.Ala259=
ENST00000480670.2:n.3669C=
ENST00000676680.1:c.600C=	ENSP00000503270.1:p.Ala200=
ENST00000676716.1:c.477C=	ENSP00000504737.1:p.Ala159=
ENST00000676751.1:c.600C=	ENSP00000502964.1:p.Ala200=
ENST00000676824.1:c.600C=	ENSP00000504176.1:p.Ala200=
ENST00000676966.1:c.600C=	ENSP00000503723.1:p.Ala200=
ENST00000676970.1:c.600C=	ENSP00000503832.1:p.Ala200=
ENST00000677330.1:n.2426C=
ENST00000677611.1:n.452C=
ENST00000677887.1:c.642C=	ENSP00000503876.1:p.Ala214=
ENST00000678275.1:c.*492C=	ENSP00000504796.1:n.*492C=
ENST00000678337.1:c.636C=	ENSP00000504759.1:p.Ala212=
ENST00000678725.1:n.1577C=
ENST00000679090.1:n.1185C=
ENST00000679148.1:n.3562C=
ENST00000679171.1:n.2961C=
ENST00000679260.1:c.399+1822C=	ENSP00000504534.1:n.399+1822C=
ENST00000271651.7:c.600C=	ENSP00000271651.3:p.Ala200=
ENST00000480670.1:n.440C=
NM_000396.3:c.600C=	NP_000387.1:p.Ala200=
NM_000396.4:c.600C= MANE Select	NP_000387.1:p.Ala200=