Canonical Allele Identifier: CA2479314208

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804106C= , CM000663.2:g.150804106C=	GRCh38
NC_000001.10:g.150776582C= , CM000663.1:g.150776582C=	GRCh37
NC_000001.9:g.149043206C=	NCBI36
NG_011848.1:g.9231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.533G= MANE Select	ENSP00000271651.3:p.Gly178=
ENST00000443913.2:c.710G=	ENSP00000405083.2:p.Gly237=
ENST00000480670.2:n.3602G=
ENST00000676680.1:c.533G=	ENSP00000503270.1:p.Gly178=
ENST00000676716.1:c.410G=	ENSP00000504737.1:p.Gly137=
ENST00000676751.1:c.533G=	ENSP00000502964.1:p.Gly178=
ENST00000676824.1:c.533G=	ENSP00000504176.1:p.Gly178=
ENST00000676966.1:c.533G=	ENSP00000503723.1:p.Gly178=
ENST00000676970.1:c.533G=	ENSP00000503832.1:p.Gly178=
ENST00000677330.1:n.2359G=
ENST00000677611.1:n.385G=
ENST00000677887.1:c.575G=	ENSP00000503876.1:p.Gly192=
ENST00000678275.1:c.*425G=	ENSP00000504796.1:n.*425G=
ENST00000678337.1:c.569G=	ENSP00000504759.1:p.Gly190=
ENST00000678725.1:n.1510G=
ENST00000679090.1:n.1118G=
ENST00000679148.1:n.3495G=
ENST00000679171.1:n.2894G=
ENST00000679260.1:c.399+1755G=	ENSP00000504534.1:n.399+1755G=
ENST00000271651.7:c.533G=	ENSP00000271651.3:p.Gly178=
ENST00000443913.1:c.710G=	ENSP00000405083.1:p.Gly237=
ENST00000480670.1:n.373G=
NM_000396.3:c.533G=	NP_000387.1:p.Gly178=
NM_000396.4:c.533G= MANE Select	NP_000387.1:p.Gly178=