Canonical Allele Identifier: CA2479314205

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804092T= , CM000663.2:g.150804092T=	GRCh38
NC_000001.10:g.150776568T= , CM000663.1:g.150776568T=	GRCh37
NC_000001.9:g.149043192T=	NCBI36
NG_011848.1:g.9245A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.547A= MANE Select	ENSP00000271651.3:p.Thr183=
ENST00000443913.2:c.724A=	ENSP00000405083.2:p.Thr242=
ENST00000480670.2:n.3616A=
ENST00000676680.1:c.547A=	ENSP00000503270.1:p.Thr183=
ENST00000676716.1:c.424A=	ENSP00000504737.1:p.Thr142=
ENST00000676751.1:c.547A=	ENSP00000502964.1:p.Thr183=
ENST00000676824.1:c.547A=	ENSP00000504176.1:p.Thr183=
ENST00000676966.1:c.547A=	ENSP00000503723.1:p.Thr183=
ENST00000676970.1:c.547A=	ENSP00000503832.1:p.Thr183=
ENST00000677330.1:n.2373A=
ENST00000677611.1:n.399A=
ENST00000677887.1:c.589A=	ENSP00000503876.1:p.Thr197=
ENST00000678275.1:c.*439A=	ENSP00000504796.1:n.*439A=
ENST00000678337.1:c.583A=	ENSP00000504759.1:p.Thr195=
ENST00000678725.1:n.1524A=
ENST00000679090.1:n.1132A=
ENST00000679148.1:n.3509A=
ENST00000679171.1:n.2908A=
ENST00000679260.1:c.399+1769A=	ENSP00000504534.1:n.399+1769A=
ENST00000271651.7:c.547A=	ENSP00000271651.3:p.Thr183=
ENST00000443913.1:c.724A=	ENSP00000405083.1:p.Thr242=
ENST00000480670.1:n.387A=
NM_000396.3:c.547A=	NP_000387.1:p.Thr183=
NM_000396.4:c.547A= MANE Select	NP_000387.1:p.Thr183=