Canonical Allele Identifier: CA2479314225
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804161_150804167delinsAGAGTTT , CM000663.2:g.150804161_150804167delinsAGAGTTT GRCh38
NC_000001.10:g.150776637_150776643delinsAGAGTTT , CM000663.1:g.150776637_150776643delinsAGAGTTT GRCh37
NC_000001.9:g.149043261_149043267delinsAGAGTTT NCBI36
NG_011848.1:g.9170_9176delinsAAACTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.472_478delinsAAACTCT MANE Select ENSP00000271651.3:p.Lys158=
ENST00000443913.2:c.649_655delinsAAACTCT ENSP00000405083.2:p.Lys217=
ENST00000480670.2:n.3541_3547delinsAAACTCT
ENST00000676680.1:c.472_478delinsAAACTCT ENSP00000503270.1:p.Lys158=
ENST00000676716.1:c.349_355delinsAAACTCT ENSP00000504737.1:p.Lys117=
ENST00000676751.1:c.472_478delinsAAACTCT ENSP00000502964.1:p.Lys158=
ENST00000676824.1:c.472_478delinsAAACTCT ENSP00000504176.1:p.Lys158=
ENST00000676966.1:c.472_478delinsAAACTCT ENSP00000503723.1:p.Lys158=
ENST00000676970.1:c.472_478delinsAAACTCT ENSP00000503832.1:p.Lys158=
ENST00000677330.1:n.2298_2304delinsAAACTCT
ENST00000677611.1:n.324_330delinsAAACTCT
ENST00000677887.1:c.514_520delinsAAACTCT ENSP00000503876.1:p.Lys172=
ENST00000678275.1:c.*364_*370delinsAAACTCT ENSP00000504796.1:n.*364_*370delinsAAACTCT
ENST00000678337.1:c.508_514delinsAAACTCT ENSP00000504759.1:p.Lys170=
ENST00000678725.1:n.1449_1455delinsAAACTCT
ENST00000679090.1:n.1057_1063delinsAAACTCT
ENST00000679148.1:n.3434_3440delinsAAACTCT
ENST00000679171.1:n.2833_2839delinsAAACTCT
ENST00000679260.1:c.399+1694_399+1700delinsAAACTCT ENSP00000504534.1:n.399+1694_399+1700delinsAAACTCT
ENST00000271651.7:c.472_478delinsAAACTCT ENSP00000271651.3:p.Lys158=
ENST00000443913.1:c.649_655delinsAAACTCT ENSP00000405083.1:p.Lys217=
ENST00000480670.1:n.312_318delinsAAACTCT
NM_000396.3:c.472_478delinsAAACTCT NP_000387.1:p.Lys158=
NM_000396.4:c.472_478delinsAAACTCT MANE Select NP_000387.1:p.Lys158=