Canonical Allele Identifier: CA1148469913

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150803977_150803984delinsAGGAGGAG , CM000663.2:g.150803977_150803984delinsAGGAGGAG	GRCh38
NC_000001.10:g.150776453_150776460delinsAGGAGGAG , CM000663.1:g.150776453_150776460delinsAGGAGGAG	GRCh37
NC_000001.9:g.149043077_149043084delinsAGGAGGAG	NCBI36
NG_011848.1:g.9353_9360delinsCTCCTCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.618+37_618+44delinsCTCCTCCT MANE Select	ENSP00000271651.3:n.618+37_618+44delinsCT...
ENST00000443913.2:c.795+37_795+44delinsCTCCTCCT	ENSP00000405083.2:n.795+37_795+44delinsCT...
ENST00000480670.2:n.3687+37_3687+44delinsCTCCTCCT
ENST00000676680.1:c.618+37_618+44delinsCTCCTCCT	ENSP00000503270.1:n.618+37_618+44delinsCT...
ENST00000676716.1:c.495+37_495+44delinsCTCCTCCT	ENSP00000504737.1:n.495+37_495+44delinsCT...
ENST00000676751.1:c.618+37_618+44delinsCTCCTCCT	ENSP00000502964.1:n.618+37_618+44delinsCT...
ENST00000676824.1:c.618+37_618+44delinsCTCCTCCT	ENSP00000504176.1:n.618+37_618+44delinsCT...
ENST00000676966.1:c.618+37_618+44delinsCTCCTCCT	ENSP00000503723.1:n.618+37_618+44delinsCT...
ENST00000676970.1:c.618+37_618+44delinsCTCCTCCT	ENSP00000503832.1:n.618+37_618+44delinsCT...
ENST00000677330.1:n.2444+37_2444+44delinsCTCCTCCT
ENST00000677611.1:n.470+37_470+44delinsCTCCTCCT
ENST00000677887.1:c.660+37_660+44delinsCTCCTCCT	ENSP00000503876.1:n.660+37_660+44delinsCT...
ENST00000678275.1:c.*510+37_*510+44delinsCTCCTCCT	ENSP00000504796.1:n.*510+37_*510+44delins...
ENST00000678337.1:c.654+37_654+44delinsCTCCTCCT	ENSP00000504759.1:n.654+37_654+44delinsCT...
ENST00000678725.1:n.1595+37_1595+44delinsCTCCTCCT
ENST00000679090.1:n.1203+37_1203+44delinsCTCCTCCT
ENST00000679148.1:n.3580+37_3580+44delinsCTCCTCCT
ENST00000679171.1:n.2979+37_2979+44delinsCTCCTCCT
ENST00000679260.1:c.399+1877_399+1884delinsCTCCTCCT	ENSP00000504534.1:n.399+1877_399+1884deli...
ENST00000271651.7:c.618+37_618+44delinsCTCCTCCT	ENSP00000271651.3:n.618+37_618+44delinsCT...
NM_000396.3:c.618+37_618+44delinsCTCCTCCT	NP_000387.1:n.618+37_618+44delinsCTCCTCCT...
NM_000396.4:c.618+37_618+44delinsCTCCTCCT MANE Select	NP_000387.1:n.618+37_618+44delinsCTCCTCCT...