Canonical Allele Identifier: CA2479314224

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804158T= , CM000663.2:g.150804158T=	GRCh38
NC_000001.10:g.150776634T= , CM000663.1:g.150776634T=	GRCh37
NC_000001.9:g.149043258T=	NCBI36
NG_011848.1:g.9179A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.481A= MANE Select	ENSP00000271651.3:p.Asn161=
ENST00000443913.2:c.658A=	ENSP00000405083.2:p.Asn220=
ENST00000480670.2:n.3550A=
ENST00000676680.1:c.481A=	ENSP00000503270.1:p.Asn161=
ENST00000676716.1:c.358A=	ENSP00000504737.1:p.Asn120=
ENST00000676751.1:c.481A=	ENSP00000502964.1:p.Asn161=
ENST00000676824.1:c.481A=	ENSP00000504176.1:p.Asn161=
ENST00000676966.1:c.481A=	ENSP00000503723.1:p.Asn161=
ENST00000676970.1:c.481A=	ENSP00000503832.1:p.Asn161=
ENST00000677330.1:n.2307A=
ENST00000677611.1:n.333A=
ENST00000677887.1:c.523A=	ENSP00000503876.1:p.Asn175=
ENST00000678275.1:c.*373A=	ENSP00000504796.1:n.*373A=
ENST00000678337.1:c.517A=	ENSP00000504759.1:p.Asn173=
ENST00000678725.1:n.1458A=
ENST00000679090.1:n.1066A=
ENST00000679148.1:n.3443A=
ENST00000679171.1:n.2842A=
ENST00000679260.1:c.399+1703A=	ENSP00000504534.1:n.399+1703A=
ENST00000271651.7:c.481A=	ENSP00000271651.3:p.Asn161=
ENST00000443913.1:c.658A=	ENSP00000405083.1:p.Asn220=
ENST00000480670.1:n.321A=
NM_000396.3:c.481A=	NP_000387.1:p.Asn161=
NM_000396.4:c.481A= MANE Select	NP_000387.1:p.Asn161=