Canonical Allele Identifier: CA342337626

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806729C>T , CM000663.2:g.150806729C>T	GRCh38
NC_000001.10:g.150779205C>T , CM000663.1:g.150779205C>T	GRCh37
NC_000001.9:g.149045829C>T	NCBI36
NG_011848.1:g.6608G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.77G>A MANE Select	NP_000387.1:p.Trp26Ter
ENST00000271651.8:c.77G>A MANE Select	ENSP00000271651.3:p.Trp26Ter
NM_000396.3:c.77G>A	NP_000387.1:p.Trp26Ter
ENST00000271651.7:c.77G>A	ENSP00000271651.3:p.Trp26Ter
ENST00000443913.1:c.254G>A	ENSP00000405083.1:p.Trp85Ter
ENST00000443913.2:c.254G>A	ENSP00000405083.2:p.Trp85Ter
ENST00000480670.1:n.40G>A
ENST00000480670.2:n.2685G>A
ENST00000676680.1:c.77G>A	ENSP00000503270.1:p.Trp26Ter
ENST00000676716.1:c.77G>A	ENSP00000504737.1:p.Trp26Ter
ENST00000676751.1:c.77G>A	ENSP00000502964.1:p.Trp26Ter
ENST00000676824.1:c.77G>A	ENSP00000504176.1:p.Trp26Ter
ENST00000676966.1:c.77G>A	ENSP00000503723.1:p.Trp26Ter
ENST00000676970.1:c.77G>A	ENSP00000503832.1:p.Trp26Ter
ENST00000677330.1:n.1442G>A
ENST00000677887.1:c.119G>A	ENSP00000503876.1:p.Trp40Ter
ENST00000678275.1:c.77G>A	ENSP00000504796.1:p.Trp26Ter
ENST00000678337.1:c.113G>A	ENSP00000504759.1:p.Trp38Ter
ENST00000678725.1:n.1054G>A
ENST00000679090.1:n.201G>A
ENST00000679148.1:n.957G>A
ENST00000679171.1:n.1977G>A
ENST00000679260.1:c.77G>A	ENSP00000504534.1:p.Trp26Ter