Canonical Allele Identifier: CA1140886763

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804203C= , CM000663.2:g.150804203C=	GRCh38
NC_000001.10:g.150776679C= , CM000663.1:g.150776679C=	GRCh37
NC_000001.9:g.149043303C=	NCBI36
NG_011848.1:g.9134G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.436G= MANE Select	ENSP00000271651.3:p.Gly146=
ENST00000443913.2:c.613G=	ENSP00000405083.2:p.Gly205=
ENST00000480670.2:n.3505G=
ENST00000676680.1:c.436G=	ENSP00000503270.1:p.Gly146=
ENST00000676716.1:c.313G=	ENSP00000504737.1:p.Gly105=
ENST00000676751.1:c.436G=	ENSP00000502964.1:p.Gly146=
ENST00000676824.1:c.436G=	ENSP00000504176.1:p.Gly146=
ENST00000676966.1:c.436G=	ENSP00000503723.1:p.Gly146=
ENST00000676970.1:c.436G=	ENSP00000503832.1:p.Gly146=
ENST00000677330.1:n.2262G=
ENST00000677611.1:n.288G=
ENST00000677887.1:c.478G=	ENSP00000503876.1:p.Gly160=
ENST00000678275.1:c.*328G=	ENSP00000504796.1:n.*328G=
ENST00000678337.1:c.472G=	ENSP00000504759.1:p.Gly158=
ENST00000678725.1:n.1413G=
ENST00000679090.1:n.1021G=
ENST00000679148.1:n.3398G=
ENST00000679171.1:n.2797G=
ENST00000679260.1:c.399+1658G=	ENSP00000504534.1:n.399+1658G=
ENST00000271651.7:c.436G=	ENSP00000271651.3:p.Gly146=
ENST00000443913.1:c.613G=	ENSP00000405083.1:p.Gly205=
ENST00000480670.1:n.276G=
NM_000396.3:c.436G=	NP_000387.1:p.Gly146=
NM_000396.4:c.436G= MANE Select	NP_000387.1:p.Gly146=