Canonical Allele Identifier: CA2479314185

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804030A= , CM000663.2:g.150804030A=	GRCh38
NC_000001.10:g.150776506A= , CM000663.1:g.150776506A=	GRCh37
NC_000001.9:g.149043130A=	NCBI36
NG_011848.1:g.9307T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.609T= MANE Select	ENSP00000271651.3:p.Tyr203=
ENST00000443913.2:c.786T=	ENSP00000405083.2:p.Tyr262=
ENST00000480670.2:n.3678T=
ENST00000676680.1:c.609T=	ENSP00000503270.1:p.Tyr203=
ENST00000676716.1:c.486T=	ENSP00000504737.1:p.Tyr162=
ENST00000676751.1:c.609T=	ENSP00000502964.1:p.Tyr203=
ENST00000676824.1:c.609T=	ENSP00000504176.1:p.Tyr203=
ENST00000676966.1:c.609T=	ENSP00000503723.1:p.Tyr203=
ENST00000676970.1:c.609T=	ENSP00000503832.1:p.Tyr203=
ENST00000677330.1:n.2435T=
ENST00000677611.1:n.461T=
ENST00000677887.1:c.651T=	ENSP00000503876.1:p.Tyr217=
ENST00000678275.1:c.*501T=	ENSP00000504796.1:n.*501T=
ENST00000678337.1:c.645T=	ENSP00000504759.1:p.Tyr215=
ENST00000678725.1:n.1586T=
ENST00000679090.1:n.1194T=
ENST00000679148.1:n.3571T=
ENST00000679171.1:n.2970T=
ENST00000679260.1:c.399+1831T=	ENSP00000504534.1:n.399+1831T=
ENST00000271651.7:c.609T=	ENSP00000271651.3:p.Tyr203=
ENST00000480670.1:n.449T=
NM_000396.3:c.609T=	NP_000387.1:p.Tyr203=
NM_000396.4:c.609T= MANE Select	NP_000387.1:p.Tyr203=