Canonical Allele Identifier: CA2574054768
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804244A>G , CM000663.2:g.150804244A>G GRCh38
NC_000001.10:g.150776720A>G , CM000663.1:g.150776720A>G GRCh37
NC_000001.9:g.149043344A>G NCBI36
NG_011848.1:g.9093T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.400-5T>C MANE Select ENSP00000271651.3:n.400-5T>C
ENST00000443913.2:c.577-5T>C ENSP00000405083.2:n.577-5T>C
ENST00000480670.2:n.3469-5T>C
ENST00000676680.1:c.400-5T>C ENSP00000503270.1:n.400-5T>C
ENST00000676716.1:c.277-5T>C ENSP00000504737.1:n.277-5T>C
ENST00000676751.1:c.400-5T>C ENSP00000502964.1:n.400-5T>C
ENST00000676824.1:c.400-5T>C ENSP00000504176.1:n.400-5T>C
ENST00000676966.1:c.400-5T>C ENSP00000503723.1:n.400-5T>C
ENST00000676970.1:c.400-5T>C ENSP00000503832.1:n.400-5T>C
ENST00000677330.1:n.2226-5T>C
ENST00000677611.1:n.252-5T>C
ENST00000677887.1:c.442-5T>C ENSP00000503876.1:n.442-5T>C
ENST00000678275.1:c.*292-5T>C ENSP00000504796.1:n.*292-5T>C
ENST00000678337.1:c.436-5T>C ENSP00000504759.1:n.436-5T>C
ENST00000678725.1:n.1377-5T>C
ENST00000679090.1:n.985-5T>C
ENST00000679148.1:n.3357T>C
ENST00000679171.1:n.2761-5T>C
ENST00000679260.1:c.399+1617T>C ENSP00000504534.1:n.399+1617T>C
ENST00000271651.7:c.400-5T>C ENSP00000271651.3:n.400-5T>C
ENST00000443913.1:c.577-5T>C ENSP00000405083.1:n.577-5T>C
ENST00000480670.1:n.240-5T>C
NM_000396.3:c.400-5T>C NP_000387.1:n.400-5T>C
NM_000396.4:c.400-5T>C MANE Select NP_000387.1:n.400-5T>C