Canonical Allele Identifier: CA2479314218

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804140G= , CM000663.2:g.150804140G=	GRCh38
NC_000001.10:g.150776616G= , CM000663.1:g.150776616G=	GRCh37
NC_000001.9:g.149043240G=	NCBI36
NG_011848.1:g.9197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.499C= MANE Select	ENSP00000271651.3:p.Leu167=
ENST00000443913.2:c.676C=	ENSP00000405083.2:p.Leu226=
ENST00000480670.2:n.3568C=
ENST00000676680.1:c.499C=	ENSP00000503270.1:p.Leu167=
ENST00000676716.1:c.376C=	ENSP00000504737.1:p.Leu126=
ENST00000676751.1:c.499C=	ENSP00000502964.1:p.Leu167=
ENST00000676824.1:c.499C=	ENSP00000504176.1:p.Leu167=
ENST00000676966.1:c.499C=	ENSP00000503723.1:p.Leu167=
ENST00000676970.1:c.499C=	ENSP00000503832.1:p.Leu167=
ENST00000677330.1:n.2325C=
ENST00000677611.1:n.351C=
ENST00000677887.1:c.541C=	ENSP00000503876.1:p.Leu181=
ENST00000678275.1:c.*391C=	ENSP00000504796.1:n.*391C=
ENST00000678337.1:c.535C=	ENSP00000504759.1:p.Leu179=
ENST00000678725.1:n.1476C=
ENST00000679090.1:n.1084C=
ENST00000679148.1:n.3461C=
ENST00000679171.1:n.2860C=
ENST00000679260.1:c.399+1721C=	ENSP00000504534.1:n.399+1721C=
ENST00000271651.7:c.499C=	ENSP00000271651.3:p.Leu167=
ENST00000443913.1:c.676C=	ENSP00000405083.1:p.Leu226=
ENST00000480670.1:n.339C=
NM_000396.3:c.499C=	NP_000387.1:p.Leu167=
NM_000396.4:c.499C= MANE Select	NP_000387.1:p.Leu167=