Canonical Allele Identifier: CA342337386

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806196C>T , CM000663.2:g.150806196C>T	GRCh38
NC_000001.10:g.150778672C>T , CM000663.1:g.150778672C>T	GRCh37
NC_000001.9:g.149045296C>T	NCBI36
NG_011848.1:g.7141G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.149G>A MANE Select	NP_000387.1:p.Trp50Ter
ENST00000271651.8:c.149G>A MANE Select	ENSP00000271651.3:p.Trp50Ter
NM_000396.3:c.149G>A	NP_000387.1:p.Trp50Ter
ENST00000271651.7:c.149G>A	ENSP00000271651.3:p.Trp50Ter
ENST00000443913.1:c.326G>A	ENSP00000405083.1:p.Trp109Ter
ENST00000443913.2:c.326G>A	ENSP00000405083.2:p.Trp109Ter
ENST00000480670.1:n.84-180G>A
ENST00000480670.2:n.3218G>A
ENST00000676680.1:c.149G>A	ENSP00000503270.1:p.Trp50Ter
ENST00000676716.1:c.121-180G>A	ENSP00000504737.1:n.121-180G>A
ENST00000676751.1:c.149G>A	ENSP00000502964.1:p.Trp50Ter
ENST00000676824.1:c.149G>A	ENSP00000504176.1:p.Trp50Ter
ENST00000676966.1:c.149G>A	ENSP00000503723.1:p.Trp50Ter
ENST00000676970.1:c.149G>A	ENSP00000503832.1:p.Trp50Ter
ENST00000677330.1:n.1975G>A
ENST00000677887.1:c.191G>A	ENSP00000503876.1:p.Trp64Ter
ENST00000678275.1:c.*41G>A	ENSP00000504796.1:n.*41G>A
ENST00000678337.1:c.185G>A	ENSP00000504759.1:p.Trp62Ter
ENST00000678725.1:n.1126G>A
ENST00000679090.1:n.734G>A
ENST00000679148.1:n.1490G>A
ENST00000679171.1:n.2510G>A
ENST00000679260.1:c.149G>A	ENSP00000504534.1:p.Trp50Ter