Canonical Allele Identifier: CA1143389628

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804073A= , CM000663.2:g.150804073A=	GRCh38
NC_000001.10:g.150776549A= , CM000663.1:g.150776549A=	GRCh37
NC_000001.9:g.149043173A=	NCBI36
NG_011848.1:g.9264T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.566T= MANE Select	ENSP00000271651.3:p.Val189=
ENST00000443913.2:c.743T=	ENSP00000405083.2:p.Val248=
ENST00000480670.2:n.3635T=
ENST00000676680.1:c.566T=	ENSP00000503270.1:p.Val189=
ENST00000676716.1:c.443T=	ENSP00000504737.1:p.Val148=
ENST00000676751.1:c.566T=	ENSP00000502964.1:p.Val189=
ENST00000676824.1:c.566T=	ENSP00000504176.1:p.Val189=
ENST00000676966.1:c.566T=	ENSP00000503723.1:p.Val189=
ENST00000676970.1:c.566T=	ENSP00000503832.1:p.Val189=
ENST00000677330.1:n.2392T=
ENST00000677611.1:n.418T=
ENST00000677887.1:c.608T=	ENSP00000503876.1:p.Val203=
ENST00000678275.1:c.*458T=	ENSP00000504796.1:n.*458T=
ENST00000678337.1:c.602T=	ENSP00000504759.1:p.Val201=
ENST00000678725.1:n.1543T=
ENST00000679090.1:n.1151T=
ENST00000679148.1:n.3528T=
ENST00000679171.1:n.2927T=
ENST00000679260.1:c.399+1788T=	ENSP00000504534.1:n.399+1788T=
ENST00000271651.7:c.566T=	ENSP00000271651.3:p.Val189=
ENST00000443913.1:c.743T=	ENSP00000405083.1:p.Val248=
ENST00000480670.1:n.406T=
NM_000396.3:c.566T=	NP_000387.1:p.Val189=
NM_000396.4:c.566T= MANE Select	NP_000387.1:p.Val189=