Canonical Allele Identifier: CA2479314220

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804145T= , CM000663.2:g.150804145T=	GRCh38
NC_000001.10:g.150776621T= , CM000663.1:g.150776621T=	GRCh37
NC_000001.9:g.149043245T=	NCBI36
NG_011848.1:g.9192A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.494A= MANE Select	ENSP00000271651.3:p.Gln165=
ENST00000443913.2:c.671A=	ENSP00000405083.2:p.Gln224=
ENST00000480670.2:n.3563A=
ENST00000676680.1:c.494A=	ENSP00000503270.1:p.Gln165=
ENST00000676716.1:c.371A=	ENSP00000504737.1:p.Gln124=
ENST00000676751.1:c.494A=	ENSP00000502964.1:p.Gln165=
ENST00000676824.1:c.494A=	ENSP00000504176.1:p.Gln165=
ENST00000676966.1:c.494A=	ENSP00000503723.1:p.Gln165=
ENST00000676970.1:c.494A=	ENSP00000503832.1:p.Gln165=
ENST00000677330.1:n.2320A=
ENST00000677611.1:n.346A=
ENST00000677887.1:c.536A=	ENSP00000503876.1:p.Gln179=
ENST00000678275.1:c.*386A=	ENSP00000504796.1:n.*386A=
ENST00000678337.1:c.530A=	ENSP00000504759.1:p.Gln177=
ENST00000678725.1:n.1471A=
ENST00000679090.1:n.1079A=
ENST00000679148.1:n.3456A=
ENST00000679171.1:n.2855A=
ENST00000679260.1:c.399+1716A=	ENSP00000504534.1:n.399+1716A=
ENST00000271651.7:c.494A=	ENSP00000271651.3:p.Gln165=
ENST00000443913.1:c.671A=	ENSP00000405083.1:p.Gln224=
ENST00000480670.1:n.334A=
NM_000396.3:c.494A=	NP_000387.1:p.Gln165=
NM_000396.4:c.494A= MANE Select	NP_000387.1:p.Gln165=