Canonical Allele Identifier: CA2697256764
Gene: CTSK HGNC NCBI

Linked Data

dbSNP Id: rs1194292135

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804258A>C , CM000663.2:g.150804258A>C GRCh38
NC_000001.10:g.150776734A>C , CM000663.1:g.150776734A>C GRCh37
NC_000001.9:g.149043358A>C NCBI36
NG_011848.1:g.9079T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.400-19T>G MANE Select ENSP00000271651.3:n.400-19T>G
ENST00000443913.2:c.577-19T>G ENSP00000405083.2:n.577-19T>G
ENST00000480670.2:n.3469-19T>G
ENST00000676680.1:c.400-19T>G ENSP00000503270.1:n.400-19T>G
ENST00000676716.1:c.277-19T>G ENSP00000504737.1:n.277-19T>G
ENST00000676751.1:c.400-19T>G ENSP00000502964.1:n.400-19T>G
ENST00000676824.1:c.400-19T>G ENSP00000504176.1:n.400-19T>G
ENST00000676966.1:c.400-19T>G ENSP00000503723.1:n.400-19T>G
ENST00000676970.1:c.400-19T>G ENSP00000503832.1:n.400-19T>G
ENST00000677330.1:n.2226-19T>G
ENST00000677611.1:n.252-19T>G
ENST00000677887.1:c.442-19T>G ENSP00000503876.1:n.442-19T>G
ENST00000678275.1:c.*292-19T>G ENSP00000504796.1:n.*292-19T>G
ENST00000678337.1:c.436-19T>G ENSP00000504759.1:n.436-19T>G
ENST00000678725.1:n.1377-19T>G
ENST00000679090.1:n.985-19T>G
ENST00000679148.1:n.3343T>G
ENST00000679171.1:n.2761-19T>G
ENST00000679260.1:c.399+1603T>G ENSP00000504534.1:n.399+1603T>G
ENST00000271651.7:c.400-19T>G ENSP00000271651.3:n.400-19T>G
ENST00000443913.1:c.577-19T>G ENSP00000405083.1:n.577-19T>G
ENST00000480670.1:n.240-19T>G
NM_000396.3:c.400-19T>G NP_000387.1:n.400-19T>G
NM_000396.4:c.400-19T>G MANE Select NP_000387.1:n.400-19T>G