Canonical Allele Identifier: CA342336080

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799607G>C , CM000663.2:g.150799607G>C	GRCh38
NC_000001.10:g.150772083G>C , CM000663.1:g.150772083G>C	GRCh37
NC_000001.9:g.149038707G>C	NCBI36
NG_011848.1:g.13730C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.721C>G MANE Select	ENSP00000271651.3:p.Arg241Gly
ENST00000443913.2:c.898C>G	ENSP00000405083.2:p.Arg300Gly
ENST00000480670.2:n.3790C>G
ENST00000676680.1:c.*15C>G	ENSP00000503270.1:n.*15C>G
ENST00000676716.1:c.598C>G	ENSP00000504737.1:p.Arg200Gly
ENST00000676751.1:c.721C>G	ENSP00000502964.1:p.Arg241Gly
ENST00000676824.1:c.721C>G	ENSP00000504176.1:p.Arg241Gly
ENST00000676966.1:c.721C>G	ENSP00000503723.1:p.Arg241Gly
ENST00000676970.1:c.721C>G	ENSP00000503832.1:p.Arg241Gly
ENST00000677330.1:n.2547C>G
ENST00000677611.1:n.573C>G
ENST00000677887.1:c.763C>G	ENSP00000503876.1:p.Arg255Gly
ENST00000678275.1:c.*613C>G	ENSP00000504796.1:n.*613C>G
ENST00000678337.1:c.757C>G	ENSP00000504759.1:p.Arg253Gly
ENST00000678725.1:n.1698C>G
ENST00000679090.1:n.1306C>G
ENST00000679148.1:n.3683C>G
ENST00000679171.1:n.3082C>G
ENST00000679178.1:n.432C>G
ENST00000679260.1:c.502C>G	ENSP00000504534.1:p.Arg168Gly
ENST00000271651.7:c.721C>G	ENSP00000271651.3:p.Arg241Gly
NM_000396.3:c.721C>G	NP_000387.1:p.Arg241Gly
NM_000396.4:c.721C>G MANE Select	NP_000387.1:p.Arg241Gly