Canonical Allele Identifier: CA2647835862
Gene: CTSK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804259_150804315dup , CM000663.2:g.150804259_150804315dup GRCh38
NC_000001.10:g.150776735_150776791dup , CM000663.1:g.150776735_150776791dup GRCh37
NC_000001.9:g.149043359_149043415dup NCBI36
NG_011848.1:g.9024_9080dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.400-74_400-18dup MANE Select ENSP00000271651.3:n.400-74_400-18dup
ENST00000443913.2:c.577-74_577-18dup ENSP00000405083.2:n.577-74_577-18dup
ENST00000480670.2:n.3469-74_3469-18dup
ENST00000676680.1:c.400-74_400-18dup ENSP00000503270.1:n.400-74_400-18dup
ENST00000676716.1:c.277-74_277-18dup ENSP00000504737.1:n.277-74_277-18dup
ENST00000676751.1:c.400-74_400-18dup ENSP00000502964.1:n.400-74_400-18dup
ENST00000676824.1:c.400-74_400-18dup ENSP00000504176.1:n.400-74_400-18dup
ENST00000676966.1:c.400-74_400-18dup ENSP00000503723.1:n.400-74_400-18dup
ENST00000676970.1:c.400-74_400-18dup ENSP00000503832.1:n.400-74_400-18dup
ENST00000677330.1:n.2226-74_2226-18dup
ENST00000677611.1:n.252-74_252-18dup
ENST00000677887.1:c.442-74_442-18dup ENSP00000503876.1:n.442-74_442-18dup
ENST00000678275.1:c.*292-74_*292-18dup ENSP00000504796.1:n.*292-74_*292-18dup
ENST00000678337.1:c.436-74_436-18dup ENSP00000504759.1:n.436-74_436-18dup
ENST00000678725.1:n.1377-74_1377-18dup
ENST00000679090.1:n.985-74_985-18dup
ENST00000679148.1:n.3288_3344dup
ENST00000679171.1:n.2761-74_2761-18dup
ENST00000679260.1:c.399+1548_399+1604dup ENSP00000504534.1:n.399+1548_399+1604dup
ENST00000271651.7:c.400-74_400-18dup ENSP00000271651.3:n.400-74_400-18dup
ENST00000443913.1:c.577-74_577-18dup ENSP00000405083.1:n.577-74_577-18dup
ENST00000480670.1:n.240-74_240-18dup
NM_000396.3:c.400-74_400-18dup NP_000387.1:n.400-74_400-18dup
NM_000396.4:c.400-74_400-18dup MANE Select NP_000387.1:n.400-74_400-18dup