Canonical Allele Identifier: CA2479314241

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804218_150804228delinsCCCAACAGGAA , CM000663.2:g.150804218_150804228delinsCCCAACAGGAA	GRCh38
NC_000001.10:g.150776694_150776704delinsCCCAACAGGAA , CM000663.1:g.150776694_150776704delinsCCCAACAGGAA	GRCh37
NC_000001.9:g.149043318_149043328delinsCCCAACAGGAA	NCBI36
NG_011848.1:g.9109_9119delinsTTCCTGTTGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.411_421delinsTTCCTGTTGGG MANE Select	ENSP00000271651.3:p.Gly137=
ENST00000443913.2:c.588_598delinsTTCCTGTTGGG	ENSP00000405083.2:p.Gly196=
ENST00000480670.2:n.3480_3490delinsTTCCTGTTGGG
ENST00000676680.1:c.411_421delinsTTCCTGTTGGG	ENSP00000503270.1:p.Gly137=
ENST00000676716.1:c.288_298delinsTTCCTGTTGGG	ENSP00000504737.1:p.Gly96=
ENST00000676751.1:c.411_421delinsTTCCTGTTGGG	ENSP00000502964.1:p.Gly137=
ENST00000676824.1:c.411_421delinsTTCCTGTTGGG	ENSP00000504176.1:p.Gly137=
ENST00000676966.1:c.411_421delinsTTCCTGTTGGG	ENSP00000503723.1:p.Gly137=
ENST00000676970.1:c.411_421delinsTTCCTGTTGGG	ENSP00000503832.1:p.Gly137=
ENST00000677330.1:n.2237_2247delinsTTCCTGTTGGG
ENST00000677611.1:n.263_273delinsTTCCTGTTGGG
ENST00000677887.1:c.453_463delinsTTCCTGTTGGG	ENSP00000503876.1:p.Gly151=
ENST00000678275.1:c.*303_*313delinsTTCCTGTTGGG	ENSP00000504796.1:n.*303_*313delinsTTCCTG...
ENST00000678337.1:c.447_457delinsTTCCTGTTGGG	ENSP00000504759.1:p.Gly149=
ENST00000678725.1:n.1388_1398delinsTTCCTGTTGGG
ENST00000679090.1:n.996_1006delinsTTCCTGTTGGG
ENST00000679148.1:n.3373_3383delinsTTCCTGTTGGG
ENST00000679171.1:n.2772_2782delinsTTCCTGTTGGG
ENST00000679260.1:c.399+1633_399+1643delinsTTCCTGTTGGG	ENSP00000504534.1:n.399+1633_399+1643deli...
ENST00000271651.7:c.411_421delinsTTCCTGTTGGG	ENSP00000271651.3:p.Gly137=
ENST00000443913.1:c.588_598delinsTTCCTGTTGGG	ENSP00000405083.1:p.Gly196=
ENST00000480670.1:n.251_261delinsTTCCTGTTGGG
NM_000396.3:c.411_421delinsTTCCTGTTGGG	NP_000387.1:p.Gly137=
NM_000396.4:c.411_421delinsTTCCTGTTGGG MANE Select	NP_000387.1:p.Gly137=