Canonical Allele Identifier: CA2479314165
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150803976_150803979delinsAAGG , CM000663.2:g.150803976_150803979delinsAAGG GRCh38
NC_000001.10:g.150776452_150776455delinsAAGG , CM000663.1:g.150776452_150776455delinsAAGG GRCh37
NC_000001.9:g.149043076_149043079delinsAAGG NCBI36
NG_011848.1:g.9358_9361delinsCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000271651.8:c.618+42_618+45delinsCCTT MANE Select ENSP00000271651.3:n.618+42_618+45delinsCC...
ENST00000443913.2:c.795+42_795+45delinsCCTT ENSP00000405083.2:n.795+42_795+45delinsCC...
ENST00000480670.2:n.3687+42_3687+45delinsCCTT
ENST00000676680.1:c.618+42_618+45delinsCCTT ENSP00000503270.1:n.618+42_618+45delinsCC...
ENST00000676716.1:c.495+42_495+45delinsCCTT ENSP00000504737.1:n.495+42_495+45delinsCC...
ENST00000676751.1:c.618+42_618+45delinsCCTT ENSP00000502964.1:n.618+42_618+45delinsCC...
ENST00000676824.1:c.618+42_618+45delinsCCTT ENSP00000504176.1:n.618+42_618+45delinsCC...
ENST00000676966.1:c.618+42_618+45delinsCCTT ENSP00000503723.1:n.618+42_618+45delinsCC...
ENST00000676970.1:c.618+42_618+45delinsCCTT ENSP00000503832.1:n.618+42_618+45delinsCC...
ENST00000677330.1:n.2444+42_2444+45delinsCCTT
ENST00000677611.1:n.470+42_470+45delinsCCTT
ENST00000677887.1:c.660+42_660+45delinsCCTT ENSP00000503876.1:n.660+42_660+45delinsCC...
ENST00000678275.1:c.*510+42_*510+45delinsCCTT ENSP00000504796.1:n.*510+42_*510+45delins...
ENST00000678337.1:c.654+42_654+45delinsCCTT ENSP00000504759.1:n.654+42_654+45delinsCC...
ENST00000678725.1:n.1595+42_1595+45delinsCCTT
ENST00000679090.1:n.1203+42_1203+45delinsCCTT
ENST00000679148.1:n.3580+42_3580+45delinsCCTT
ENST00000679171.1:n.2979+42_2979+45delinsCCTT
ENST00000679260.1:c.399+1882_399+1885delinsCCTT ENSP00000504534.1:n.399+1882_399+1885deli...
ENST00000271651.7:c.618+42_618+45delinsCCTT ENSP00000271651.3:n.618+42_618+45delinsCC...
NM_000396.3:c.618+42_618+45delinsCCTT NP_000387.1:n.618+42_618+45delinsCCTT
NM_000396.4:c.618+42_618+45delinsCCTT MANE Select NP_000387.1:n.618+42_618+45delinsCCTT