Canonical Allele Identifier: CA2479314199

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804079T= , CM000663.2:g.150804079T=	GRCh38
NC_000001.10:g.150776555T= , CM000663.1:g.150776555T=	GRCh37
NC_000001.9:g.149043179T=	NCBI36
NG_011848.1:g.9258A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.560A= MANE Select	ENSP00000271651.3:p.Gln187=
ENST00000443913.2:c.737A=	ENSP00000405083.2:p.Gln246=
ENST00000480670.2:n.3629A=
ENST00000676680.1:c.560A=	ENSP00000503270.1:p.Gln187=
ENST00000676716.1:c.437A=	ENSP00000504737.1:p.Gln146=
ENST00000676751.1:c.560A=	ENSP00000502964.1:p.Gln187=
ENST00000676824.1:c.560A=	ENSP00000504176.1:p.Gln187=
ENST00000676966.1:c.560A=	ENSP00000503723.1:p.Gln187=
ENST00000676970.1:c.560A=	ENSP00000503832.1:p.Gln187=
ENST00000677330.1:n.2386A=
ENST00000677611.1:n.412A=
ENST00000677887.1:c.602A=	ENSP00000503876.1:p.Gln201=
ENST00000678275.1:c.*452A=	ENSP00000504796.1:n.*452A=
ENST00000678337.1:c.596A=	ENSP00000504759.1:p.Gln199=
ENST00000678725.1:n.1537A=
ENST00000679090.1:n.1145A=
ENST00000679148.1:n.3522A=
ENST00000679171.1:n.2921A=
ENST00000679260.1:c.399+1782A=	ENSP00000504534.1:n.399+1782A=
ENST00000271651.7:c.560A=	ENSP00000271651.3:p.Gln187=
ENST00000443913.1:c.737A=	ENSP00000405083.1:p.Gln246=
ENST00000480670.1:n.400A=
NM_000396.3:c.560A=	NP_000387.1:p.Gln187=
NM_000396.4:c.560A= MANE Select	NP_000387.1:p.Gln187=