Canonical Allele Identifier: CA1140886765

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806191T= , CM000663.2:g.150806191T=	GRCh38
NC_000001.10:g.150778667T= , CM000663.1:g.150778667T=	GRCh37
NC_000001.9:g.149045291T=	NCBI36
NG_011848.1:g.7146A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.154A= MANE Select	ENSP00000271651.3:p.Lys52=
ENST00000443913.2:c.331A=	ENSP00000405083.2:p.Lys111=
ENST00000480670.2:n.3223A=
ENST00000676680.1:c.154A=	ENSP00000503270.1:p.Lys52=
ENST00000676716.1:c.121-175A=	ENSP00000504737.1:n.121-175A=
ENST00000676751.1:c.154A=	ENSP00000502964.1:p.Lys52=
ENST00000676824.1:c.154A=	ENSP00000504176.1:p.Lys52=
ENST00000676966.1:c.154A=	ENSP00000503723.1:p.Lys52=
ENST00000676970.1:c.154A=	ENSP00000503832.1:p.Lys52=
ENST00000677330.1:n.1980A=
ENST00000677887.1:c.196A=	ENSP00000503876.1:p.Lys66=
ENST00000678275.1:c.*46A=	ENSP00000504796.1:n.*46A=
ENST00000678337.1:c.190A=	ENSP00000504759.1:p.Lys64=
ENST00000678725.1:n.1131A=
ENST00000679090.1:n.739A=
ENST00000679148.1:n.1495A=
ENST00000679171.1:n.2515A=
ENST00000679260.1:c.154A=	ENSP00000504534.1:p.Lys52=
ENST00000271651.7:c.154A=	ENSP00000271651.3:p.Lys52=
ENST00000443913.1:c.331A=	ENSP00000405083.1:p.Lys111=
ENST00000480670.1:n.84-175A=
NM_000396.3:c.154A=	NP_000387.1:p.Lys52=
NM_000396.4:c.154A= MANE Select	NP_000387.1:p.Lys52=