Canonical Allele Identifier: CA2479314217

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804139A= , CM000663.2:g.150804139A=	GRCh38
NC_000001.10:g.150776615A= , CM000663.1:g.150776615A=	GRCh37
NC_000001.9:g.149043239A=	NCBI36
NG_011848.1:g.9198T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.500T= MANE Select	ENSP00000271651.3:p.Leu167=
ENST00000443913.2:c.677T=	ENSP00000405083.2:p.Leu226=
ENST00000480670.2:n.3569T=
ENST00000676680.1:c.500T=	ENSP00000503270.1:p.Leu167=
ENST00000676716.1:c.377T=	ENSP00000504737.1:p.Leu126=
ENST00000676751.1:c.500T=	ENSP00000502964.1:p.Leu167=
ENST00000676824.1:c.500T=	ENSP00000504176.1:p.Leu167=
ENST00000676966.1:c.500T=	ENSP00000503723.1:p.Leu167=
ENST00000676970.1:c.500T=	ENSP00000503832.1:p.Leu167=
ENST00000677330.1:n.2326T=
ENST00000677611.1:n.352T=
ENST00000677887.1:c.542T=	ENSP00000503876.1:p.Leu181=
ENST00000678275.1:c.*392T=	ENSP00000504796.1:n.*392T=
ENST00000678337.1:c.536T=	ENSP00000504759.1:p.Leu179=
ENST00000678725.1:n.1477T=
ENST00000679090.1:n.1085T=
ENST00000679148.1:n.3462T=
ENST00000679171.1:n.2861T=
ENST00000679260.1:c.399+1722T=	ENSP00000504534.1:n.399+1722T=
ENST00000271651.7:c.500T=	ENSP00000271651.3:p.Leu167=
ENST00000443913.1:c.677T=	ENSP00000405083.1:p.Leu226=
ENST00000480670.1:n.340T=
NM_000396.3:c.500T=	NP_000387.1:p.Leu167=
NM_000396.4:c.500T= MANE Select	NP_000387.1:p.Leu167=