Canonical Allele Identifier: CA342335669

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796895C>T , CM000663.2:g.150796895C>T	GRCh38
NC_000001.10:g.150769371C>T , CM000663.1:g.150769371C>T	GRCh37
NC_000001.9:g.149035995C>T	NCBI36
NG_011848.1:g.16442G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.894G>A MANE Select	NP_000387.1:p.Trp298Ter
ENST00000271651.8:c.894G>A MANE Select	ENSP00000271651.3:p.Trp298Ter
NM_000396.3:c.894G>A	NP_000387.1:p.Trp298Ter
ENST00000271651.7:c.894G>A	ENSP00000271651.3:p.Trp298Ter
ENST00000443913.2:c.1071G>A	ENSP00000405083.2:p.Trp357Ter
ENST00000480670.2:n.3963G>A
ENST00000676680.1:c.*188G>A	ENSP00000503270.1:n.*188G>A
ENST00000676716.1:c.771G>A	ENSP00000504737.1:p.Trp257Ter
ENST00000676751.1:c.788G>A	ENSP00000502964.1:p.Gly263Glu
ENST00000676824.1:c.894G>A	ENSP00000504176.1:p.Trp298Ter
ENST00000676966.1:c.894G>A	ENSP00000503723.1:p.Trp298Ter
ENST00000676970.1:c.906G>A	ENSP00000503832.1:p.Trp302Ter
ENST00000677330.1:n.2720G>A
ENST00000677611.1:n.746G>A
ENST00000677887.1:c.936G>A	ENSP00000503876.1:p.Trp312Ter
ENST00000678275.1:c.*786G>A	ENSP00000504796.1:n.*786G>A
ENST00000678337.1:c.930G>A	ENSP00000504759.1:p.Trp310Ter
ENST00000678725.1:n.2141G>A
ENST00000679090.1:n.1749G>A
ENST00000679148.1:n.3856G>A
ENST00000679171.1:n.3525G>A
ENST00000679178.1:n.605G>A
ENST00000679260.1:c.675G>A	ENSP00000504534.1:p.Trp225Ter