Canonical Allele Identifier: CA342335834

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799232G>A , CM000663.2:g.150799232G>A	GRCh38
NC_000001.10:g.150771708G>A , CM000663.1:g.150771708G>A	GRCh37
NC_000001.9:g.149038332G>A	NCBI36
NG_011848.1:g.14105C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.826C>T MANE Select	NP_000387.1:p.His276Tyr
ENST00000271651.8:c.826C>T MANE Select	ENSP00000271651.3:p.His276Tyr
NM_000396.3:c.826C>T	NP_000387.1:p.His276Tyr
ENST00000271651.7:c.826C>T	ENSP00000271651.3:p.His276Tyr
ENST00000443913.2:c.1003C>T	ENSP00000405083.2:p.His335Tyr
ENST00000480670.2:n.3895C>T
ENST00000676680.1:c.*120C>T	ENSP00000503270.1:n.*120C>T
ENST00000676716.1:c.703C>T	ENSP00000504737.1:p.His235Tyr
ENST00000676751.1:c.784+312C>T	ENSP00000502964.1:n.784+312C>T
ENST00000676824.1:c.826C>T	ENSP00000504176.1:p.His276Tyr
ENST00000676966.1:c.826C>T	ENSP00000503723.1:p.His276Tyr
ENST00000676970.1:c.838C>T	ENSP00000503832.1:p.His280Tyr
ENST00000677330.1:n.2652C>T
ENST00000677611.1:n.678C>T
ENST00000677887.1:c.868C>T	ENSP00000503876.1:p.His290Tyr
ENST00000678275.1:c.*718C>T	ENSP00000504796.1:n.*718C>T
ENST00000678337.1:c.862C>T	ENSP00000504759.1:p.His288Tyr
ENST00000678725.1:n.2073C>T
ENST00000679090.1:n.1681C>T
ENST00000679148.1:n.3788C>T
ENST00000679171.1:n.3457C>T
ENST00000679178.1:n.537C>T
ENST00000679260.1:c.607C>T	ENSP00000504534.1:p.His203Tyr