Canonical Allele Identifier: CA2479314237

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804208G= , CM000663.2:g.150804208G=	GRCh38
NC_000001.10:g.150776684G= , CM000663.1:g.150776684G=	GRCh37
NC_000001.9:g.149043308G=	NCBI36
NG_011848.1:g.9129C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.431C= MANE Select	ENSP00000271651.3:p.Ser144=
ENST00000443913.2:c.608C=	ENSP00000405083.2:p.Ser203=
ENST00000480670.2:n.3500C=
ENST00000676680.1:c.431C=	ENSP00000503270.1:p.Ser144=
ENST00000676716.1:c.308C=	ENSP00000504737.1:p.Ser103=
ENST00000676751.1:c.431C=	ENSP00000502964.1:p.Ser144=
ENST00000676824.1:c.431C=	ENSP00000504176.1:p.Ser144=
ENST00000676966.1:c.431C=	ENSP00000503723.1:p.Ser144=
ENST00000676970.1:c.431C=	ENSP00000503832.1:p.Ser144=
ENST00000677330.1:n.2257C=
ENST00000677611.1:n.283C=
ENST00000677887.1:c.473C=	ENSP00000503876.1:p.Ser158=
ENST00000678275.1:c.*323C=	ENSP00000504796.1:n.*323C=
ENST00000678337.1:c.467C=	ENSP00000504759.1:p.Ser156=
ENST00000678725.1:n.1408C=
ENST00000679090.1:n.1016C=
ENST00000679148.1:n.3393C=
ENST00000679171.1:n.2792C=
ENST00000679260.1:c.399+1653C=	ENSP00000504534.1:n.399+1653C=
ENST00000271651.7:c.431C=	ENSP00000271651.3:p.Ser144=
ENST00000443913.1:c.608C=	ENSP00000405083.1:p.Ser203=
ENST00000480670.1:n.271C=
NM_000396.3:c.431C=	NP_000387.1:p.Ser144=
NM_000396.4:c.431C= MANE Select	NP_000387.1:p.Ser144=