Canonical Allele Identifier: CA1140495879

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796863A= , CM000663.2:g.150796863A=	GRCh38
NC_000001.10:g.150769339A= , CM000663.1:g.150769339A=	GRCh37
NC_000001.9:g.149035963A=	NCBI36
NG_011848.1:g.16474T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.926T= MANE Select	ENSP00000271651.3:p.Leu309=
ENST00000443913.2:c.1103T=	ENSP00000405083.2:p.Leu368=
ENST00000480670.2:n.3995T=
ENST00000676680.1:c.*220T=	ENSP00000503270.1:n.*220T=
ENST00000676716.1:c.803T=	ENSP00000504737.1:p.Leu268=
ENST00000676751.1:c.820T=	ENSP00000502964.1:p.Ser274=
ENST00000676824.1:c.926T=	ENSP00000504176.1:p.Leu309=
ENST00000676966.1:c.926T=	ENSP00000503723.1:p.Leu309=
ENST00000676970.1:c.938T=	ENSP00000503832.1:p.Leu313=
ENST00000677330.1:n.2752T=
ENST00000677611.1:n.778T=
ENST00000677887.1:c.968T=	ENSP00000503876.1:p.Leu323=
ENST00000678275.1:c.*818T=	ENSP00000504796.1:n.*818T=
ENST00000678337.1:c.962T=	ENSP00000504759.1:p.Leu321=
ENST00000678725.1:n.2173T=
ENST00000679090.1:n.1781T=
ENST00000679148.1:n.3888T=
ENST00000679171.1:n.3557T=
ENST00000679178.1:n.637T=
ENST00000679260.1:c.707T=	ENSP00000504534.1:p.Leu236=
ENST00000271651.7:c.926T=	ENSP00000271651.3:p.Leu309=
NM_000396.3:c.926T=	NP_000387.1:p.Leu309=
NM_000396.4:c.926T= MANE Select	NP_000387.1:p.Leu309=