Canonical Allele Identifier: CA2479315140
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150806580T= , CM000663.2:g.150806580T= GRCh38
NC_000001.10:g.150779056T= , CM000663.1:g.150779056T= GRCh37
NC_000001.9:g.149045680T= NCBI36
NG_011848.1:g.6757A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.120+106A= MANE Select ENSP00000271651.3:n.120+106A=
ENST00000443913.2:c.297+106A= ENSP00000405083.2:n.297+106A=
ENST00000480670.2:n.2834A=
ENST00000676680.1:c.120+106A= ENSP00000503270.1:n.120+106A=
ENST00000676716.1:c.120+106A= ENSP00000504737.1:n.120+106A=
ENST00000676751.1:c.120+106A= ENSP00000502964.1:n.120+106A=
ENST00000676824.1:c.120+106A= ENSP00000504176.1:n.120+106A=
ENST00000676966.1:c.120+106A= ENSP00000503723.1:n.120+106A=
ENST00000676970.1:c.120+106A= ENSP00000503832.1:n.120+106A=
ENST00000677330.1:n.1591A=
ENST00000677887.1:c.162+106A= ENSP00000503876.1:n.162+106A=
ENST00000678275.1:c.120+106A= ENSP00000504796.1:n.120+106A=
ENST00000678337.1:c.156+106A= ENSP00000504759.1:n.156+106A=
ENST00000678725.1:n.1097+106A=
ENST00000679090.1:n.350A=
ENST00000679148.1:n.1106A=
ENST00000679171.1:n.2126A=
ENST00000679260.1:c.120+106A= ENSP00000504534.1:n.120+106A=
ENST00000271651.7:c.120+106A= ENSP00000271651.3:n.120+106A=
ENST00000443913.1:c.297+106A= ENSP00000405083.1:n.297+106A=
ENST00000480670.1:n.83+106A=
NM_000396.3:c.120+106A= NP_000387.1:n.120+106A=
NM_000396.4:c.120+106A= MANE Select NP_000387.1:n.120+106A=