Canonical Allele Identifier: CA342335637

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796884C>G , CM000663.2:g.150796884C>G	GRCh38
NC_000001.10:g.150769360C>G , CM000663.1:g.150769360C>G	GRCh37
NC_000001.9:g.149035984C>G	NCBI36
NG_011848.1:g.16453G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.905G>C MANE Select	NP_000387.1:p.Trp302Ser
ENST00000271651.8:c.905G>C MANE Select	ENSP00000271651.3:p.Trp302Ser
NM_000396.3:c.905G>C	NP_000387.1:p.Trp302Ser
ENST00000271651.7:c.905G>C	ENSP00000271651.3:p.Trp302Ser
ENST00000443913.2:c.1082G>C	ENSP00000405083.2:p.Trp361Ser
ENST00000480670.2:n.3974G>C
ENST00000676680.1:c.*199G>C	ENSP00000503270.1:n.*199G>C
ENST00000676716.1:c.782G>C	ENSP00000504737.1:p.Trp261Ser
ENST00000676751.1:c.799G>C	ENSP00000502964.1:p.Gly267Arg
ENST00000676824.1:c.905G>C	ENSP00000504176.1:p.Trp302Ser
ENST00000676966.1:c.905G>C	ENSP00000503723.1:p.Trp302Ser
ENST00000676970.1:c.917G>C	ENSP00000503832.1:p.Trp306Ser
ENST00000677330.1:n.2731G>C
ENST00000677611.1:n.757G>C
ENST00000677887.1:c.947G>C	ENSP00000503876.1:p.Trp316Ser
ENST00000678275.1:c.*797G>C	ENSP00000504796.1:n.*797G>C
ENST00000678337.1:c.941G>C	ENSP00000504759.1:p.Trp314Ser
ENST00000678725.1:n.2152G>C
ENST00000679090.1:n.1760G>C
ENST00000679148.1:n.3867G>C
ENST00000679171.1:n.3536G>C
ENST00000679178.1:n.616G>C
ENST00000679260.1:c.686G>C	ENSP00000504534.1:p.Trp229Ser