Canonical Allele Identifier: CA2479314172
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150803995T= , CM000663.2:g.150803995T= GRCh38
NC_000001.10:g.150776471T= , CM000663.1:g.150776471T= GRCh37
NC_000001.9:g.149043095T= NCBI36
NG_011848.1:g.9342A=

Transcript Alleles

HGVS Amino-acid change
ENST00000271651.8:c.618+26A= MANE Select ENSP00000271651.3:n.618+26A=
ENST00000443913.2:c.795+26A= ENSP00000405083.2:n.795+26A=
ENST00000480670.2:n.3687+26A=
ENST00000676680.1:c.618+26A= ENSP00000503270.1:n.618+26A=
ENST00000676716.1:c.495+26A= ENSP00000504737.1:n.495+26A=
ENST00000676751.1:c.618+26A= ENSP00000502964.1:n.618+26A=
ENST00000676824.1:c.618+26A= ENSP00000504176.1:n.618+26A=
ENST00000676966.1:c.618+26A= ENSP00000503723.1:n.618+26A=
ENST00000676970.1:c.618+26A= ENSP00000503832.1:n.618+26A=
ENST00000677330.1:n.2444+26A=
ENST00000677611.1:n.470+26A=
ENST00000677887.1:c.660+26A= ENSP00000503876.1:n.660+26A=
ENST00000678275.1:c.*510+26A= ENSP00000504796.1:n.*510+26A=
ENST00000678337.1:c.654+26A= ENSP00000504759.1:n.654+26A=
ENST00000678725.1:n.1595+26A=
ENST00000679090.1:n.1203+26A=
ENST00000679148.1:n.3580+26A=
ENST00000679171.1:n.2979+26A=
ENST00000679260.1:c.399+1866A= ENSP00000504534.1:n.399+1866A=
ENST00000271651.7:c.618+26A= ENSP00000271651.3:n.618+26A=
NM_000396.3:c.618+26A= NP_000387.1:n.618+26A=
NM_000396.4:c.618+26A= MANE Select NP_000387.1:n.618+26A=