Canonical Allele Identifier: CA1007657047
Gene: CTSK HGNC NCBI

Linked Data

dbSNP Id: rs1654043546

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804149dup , CM000663.2:g.150804149dup GRCh38
NC_000001.10:g.150776625dup , CM000663.1:g.150776625dup GRCh37
NC_000001.9:g.149043249dup NCBI36
NG_011848.1:g.9191dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.493dup MANE Select ENSP00000271651.3:p.Gln165ProfsTer9
ENST00000443913.2:c.670dup ENSP00000405083.2:p.Gln224ProfsTer9
ENST00000480670.2:n.3562dup
ENST00000676680.1:c.493dup ENSP00000503270.1:p.Gln165ProfsTer9
ENST00000676716.1:c.370dup ENSP00000504737.1:p.Gln124ProfsTer9
ENST00000676751.1:c.493dup ENSP00000502964.1:p.Gln165ProfsTer9
ENST00000676824.1:c.493dup ENSP00000504176.1:p.Gln165ProfsTer9
ENST00000676966.1:c.493dup ENSP00000503723.1:p.Gln165ProfsTer9
ENST00000676970.1:c.493dup ENSP00000503832.1:p.Gln165ProfsTer9
ENST00000677330.1:n.2319dup
ENST00000677611.1:n.345dup
ENST00000677887.1:c.535dup ENSP00000503876.1:p.Gln179ProfsTer9
ENST00000678275.1:c.*385dup ENSP00000504796.1:n.*385dup
ENST00000678337.1:c.529dup ENSP00000504759.1:p.Gln177ProfsTer9
ENST00000678725.1:n.1470dup
ENST00000679090.1:n.1078dup
ENST00000679148.1:n.3455dup
ENST00000679171.1:n.2854dup
ENST00000679260.1:c.399+1715dup ENSP00000504534.1:n.399+1715dup
ENST00000271651.7:c.493dup ENSP00000271651.3:p.Gln165ProfsTer9
ENST00000443913.1:c.670dup ENSP00000405083.1:p.Gln224ProfsTer9
ENST00000480670.1:n.333dup
NM_000396.3:c.493dup NP_000387.1:p.Gln165ProfsTer9
NM_000396.4:c.493dup MANE Select NP_000387.1:p.Gln165ProfsTer9