Canonical Allele Identifier: CA1143398132

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804144C= , CM000663.2:g.150804144C=	GRCh38
NC_000001.10:g.150776620C= , CM000663.1:g.150776620C=	GRCh37
NC_000001.9:g.149043244C=	NCBI36
NG_011848.1:g.9193G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.495G= MANE Select	ENSP00000271651.3:p.Gln165=
ENST00000443913.2:c.672G=	ENSP00000405083.2:p.Gln224=
ENST00000480670.2:n.3564G=
ENST00000676680.1:c.495G=	ENSP00000503270.1:p.Gln165=
ENST00000676716.1:c.372G=	ENSP00000504737.1:p.Gln124=
ENST00000676751.1:c.495G=	ENSP00000502964.1:p.Gln165=
ENST00000676824.1:c.495G=	ENSP00000504176.1:p.Gln165=
ENST00000676966.1:c.495G=	ENSP00000503723.1:p.Gln165=
ENST00000676970.1:c.495G=	ENSP00000503832.1:p.Gln165=
ENST00000677330.1:n.2321G=
ENST00000677611.1:n.347G=
ENST00000677887.1:c.537G=	ENSP00000503876.1:p.Gln179=
ENST00000678275.1:c.*387G=	ENSP00000504796.1:n.*387G=
ENST00000678337.1:c.531G=	ENSP00000504759.1:p.Gln177=
ENST00000678725.1:n.1472G=
ENST00000679090.1:n.1080G=
ENST00000679148.1:n.3457G=
ENST00000679171.1:n.2856G=
ENST00000679260.1:c.399+1717G=	ENSP00000504534.1:n.399+1717G=
ENST00000271651.7:c.495G=	ENSP00000271651.3:p.Gln165=
ENST00000443913.1:c.672G=	ENSP00000405083.1:p.Gln224=
ENST00000480670.1:n.335G=
NM_000396.3:c.495G=	NP_000387.1:p.Gln165=
NM_000396.4:c.495G= MANE Select	NP_000387.1:p.Gln165=