Canonical Allele Identifier: CA1141653790
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150806776A= , CM000663.2:g.150806776A= GRCh38
NC_000001.10:g.150779252A= , CM000663.1:g.150779252A= GRCh37
NC_000001.9:g.149045876A= NCBI36
NG_011848.1:g.6561T=

Transcript Alleles

HGVS Amino-acid change
ENST00000271651.8:c.30T= MANE Select ENSP00000271651.3:p.Pro10=
ENST00000443913.2:c.207T= ENSP00000405083.2:p.Pro69=
ENST00000480670.2:n.2638T=
ENST00000676680.1:c.30T= ENSP00000503270.1:p.Pro10=
ENST00000676716.1:c.30T= ENSP00000504737.1:p.Pro10=
ENST00000676751.1:c.30T= ENSP00000502964.1:p.Pro10=
ENST00000676824.1:c.30T= ENSP00000504176.1:p.Pro10=
ENST00000676966.1:c.30T= ENSP00000503723.1:p.Pro10=
ENST00000676970.1:c.30T= ENSP00000503832.1:p.Pro10=
ENST00000677330.1:n.1395T=
ENST00000677887.1:c.72T= ENSP00000503876.1:p.Pro24=
ENST00000678275.1:c.30T= ENSP00000504796.1:p.Pro10=
ENST00000678337.1:c.66T= ENSP00000504759.1:p.Pro22=
ENST00000678725.1:n.1007T=
ENST00000679090.1:n.154T=
ENST00000679148.1:n.910T=
ENST00000679171.1:n.1930T=
ENST00000679260.1:c.30T= ENSP00000504534.1:p.Pro10=
ENST00000271651.7:c.30T= ENSP00000271651.3:p.Pro10=
ENST00000443913.1:c.207T= ENSP00000405083.1:p.Pro69=
NM_000396.3:c.30T= NP_000387.1:p.Pro10=
NM_000396.4:c.30T= MANE Select NP_000387.1:p.Pro10=