Canonical Allele Identifier: CA1140886774

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799228G= , CM000663.2:g.150799228G=	GRCh38
NC_000001.10:g.150771704G= , CM000663.1:g.150771704G=	GRCh37
NC_000001.9:g.149038328G=	NCBI36
NG_011848.1:g.14109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.830C= MANE Select	ENSP00000271651.3:p.Ala277=
ENST00000443913.2:c.1007C=	ENSP00000405083.2:p.Ala336=
ENST00000480670.2:n.3899C=
ENST00000676680.1:c.*124C=	ENSP00000503270.1:n.*124C=
ENST00000676716.1:c.707C=	ENSP00000504737.1:p.Ala236=
ENST00000676751.1:c.784+316C=	ENSP00000502964.1:n.784+316C=
ENST00000676824.1:c.830C=	ENSP00000504176.1:p.Ala277=
ENST00000676966.1:c.830C=	ENSP00000503723.1:p.Ala277=
ENST00000676970.1:c.842C=	ENSP00000503832.1:p.Ala281=
ENST00000677330.1:n.2656C=
ENST00000677611.1:n.682C=
ENST00000677887.1:c.872C=	ENSP00000503876.1:p.Ala291=
ENST00000678275.1:c.*722C=	ENSP00000504796.1:n.*722C=
ENST00000678337.1:c.866C=	ENSP00000504759.1:p.Ala289=
ENST00000678725.1:n.2077C=
ENST00000679090.1:n.1685C=
ENST00000679148.1:n.3792C=
ENST00000679171.1:n.3461C=
ENST00000679178.1:n.541C=
ENST00000679260.1:c.611C=	ENSP00000504534.1:p.Ala204=
ENST00000271651.7:c.830C=	ENSP00000271651.3:p.Ala277=
NM_000396.3:c.830C=	NP_000387.1:p.Ala277=
NM_000396.4:c.830C= MANE Select	NP_000387.1:p.Ala277=