Canonical Allele Identifier: CA2479314246

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804240C= , CM000663.2:g.150804240C=	GRCh38
NC_000001.10:g.150776716C= , CM000663.1:g.150776716C=	GRCh37
NC_000001.9:g.149043340C=	NCBI36
NG_011848.1:g.9097G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.400-1G= MANE Select	ENSP00000271651.3:n.400-1G=
ENST00000443913.2:c.577-1G=	ENSP00000405083.2:n.577-1G=
ENST00000480670.2:n.3469-1G=
ENST00000676680.1:c.400-1G=	ENSP00000503270.1:n.400-1G=
ENST00000676716.1:c.277-1G=	ENSP00000504737.1:n.277-1G=
ENST00000676751.1:c.400-1G=	ENSP00000502964.1:n.400-1G=
ENST00000676824.1:c.400-1G=	ENSP00000504176.1:n.400-1G=
ENST00000676966.1:c.400-1G=	ENSP00000503723.1:n.400-1G=
ENST00000676970.1:c.400-1G=	ENSP00000503832.1:n.400-1G=
ENST00000677330.1:n.2226-1G=
ENST00000677611.1:n.252-1G=
ENST00000677887.1:c.442-1G=	ENSP00000503876.1:n.442-1G=
ENST00000678275.1:c.*292-1G=	ENSP00000504796.1:n.*292-1G=
ENST00000678337.1:c.436-1G=	ENSP00000504759.1:n.436-1G=
ENST00000678725.1:n.1377-1G=
ENST00000679090.1:n.985-1G=
ENST00000679148.1:n.3361G=
ENST00000679171.1:n.2761-1G=
ENST00000679260.1:c.399+1621G=	ENSP00000504534.1:n.399+1621G=
ENST00000271651.7:c.400-1G=	ENSP00000271651.3:n.400-1G=
ENST00000443913.1:c.577-1G=	ENSP00000405083.1:n.577-1G=
ENST00000480670.1:n.240-1G=
NM_000396.3:c.400-1G=	NP_000387.1:n.400-1G=
NM_000396.4:c.400-1G= MANE Select	NP_000387.1:n.400-1G=