Canonical Allele Identifier: CA2499214164

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799227_150799228delinsCA , CM000663.2:g.150799227_150799228delinsCA	GRCh38
NC_000001.10:g.150771703_150771704delinsCA , CM000663.1:g.150771703_150771704delinsCA	GRCh37
NC_000001.9:g.149038327_149038328delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.830_831delinsTG MANE Select	ENSP00000271651.3:p.Ala277Val
ENST00000443913.2:c.1007_1008delinsTG	ENSP00000405083.2:p.Ala336Val
ENST00000480670.2:n.3899_3900delinsTG
ENST00000676680.1:c.*124_*125delinsTG	ENSP00000503270.1:n.*124_*125delinsTG
ENST00000676716.1:c.707_708delinsTG	ENSP00000504737.1:p.Ala236Val
ENST00000676751.1:c.784+316_784+317delinsTG	ENSP00000502964.1:n.784+316_784+317delinsTG
ENST00000676824.1:c.830_831delinsTG	ENSP00000504176.1:p.Ala277Val
ENST00000676966.1:c.830_831delinsTG	ENSP00000503723.1:p.Ala277Val
ENST00000676970.1:c.842_843delinsTG	ENSP00000503832.1:p.Ala281Val
ENST00000677330.1:n.2656_2657delinsTG
ENST00000677611.1:n.682_683delinsTG
ENST00000677887.1:c.872_873delinsTG	ENSP00000503876.1:p.Ala291Val
ENST00000678275.1:c.*722_*723delinsTG	ENSP00000504796.1:n.*722_*723delinsTG
ENST00000678337.1:c.866_867delinsTG	ENSP00000504759.1:p.Ala289Val
ENST00000678725.1:n.2077_2078delinsTG
ENST00000679090.1:n.1685_1686delinsTG
ENST00000679148.1:n.3792_3793delinsTG
ENST00000679171.1:n.3461_3462delinsTG
ENST00000679178.1:n.541_542delinsTG
ENST00000679260.1:c.611_612delinsTG	ENSP00000504534.1:p.Ala204Val
ENST00000271651.7:c.830_831delinsTG	ENSP00000271651.3:p.Ala277Val
NM_000396.4:c.830_831delinsTG MANE Select	NP_000387.1:p.Ala277Val