Canonical Allele Identifier: CA2479314190

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804045T= , CM000663.2:g.150804045T=	GRCh38
NC_000001.10:g.150776521T= , CM000663.1:g.150776521T=	GRCh37
NC_000001.9:g.149043145T=	NCBI36
NG_011848.1:g.9292A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.594A= MANE Select	ENSP00000271651.3:p.Glu198=
ENST00000443913.2:c.771A=	ENSP00000405083.2:p.Glu257=
ENST00000480670.2:n.3663A=
ENST00000676680.1:c.594A=	ENSP00000503270.1:p.Glu198=
ENST00000676716.1:c.471A=	ENSP00000504737.1:p.Glu157=
ENST00000676751.1:c.594A=	ENSP00000502964.1:p.Glu198=
ENST00000676824.1:c.594A=	ENSP00000504176.1:p.Glu198=
ENST00000676966.1:c.594A=	ENSP00000503723.1:p.Glu198=
ENST00000676970.1:c.594A=	ENSP00000503832.1:p.Glu198=
ENST00000677330.1:n.2420A=
ENST00000677611.1:n.446A=
ENST00000677887.1:c.636A=	ENSP00000503876.1:p.Glu212=
ENST00000678275.1:c.*486A=	ENSP00000504796.1:n.*486A=
ENST00000678337.1:c.630A=	ENSP00000504759.1:p.Glu210=
ENST00000678725.1:n.1571A=
ENST00000679090.1:n.1179A=
ENST00000679148.1:n.3556A=
ENST00000679171.1:n.2955A=
ENST00000679260.1:c.399+1816A=	ENSP00000504534.1:n.399+1816A=
ENST00000271651.7:c.594A=	ENSP00000271651.3:p.Glu198=
ENST00000443913.1:c.771A=	ENSP00000405083.1:p.Glu257=
ENST00000480670.1:n.434A=
NM_000396.3:c.594A=	NP_000387.1:p.Glu198=
NM_000396.4:c.594A= MANE Select	NP_000387.1:p.Glu198=