Canonical Allele Identifier: CA1140886764

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806109C= , CM000663.2:g.150806109C=	GRCh38
NC_000001.10:g.150778585C= , CM000663.1:g.150778585C=	GRCh37
NC_000001.9:g.149045209C=	NCBI36
NG_011848.1:g.7228G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.236G= MANE Select	NP_000387.1:p.Gly79=
ENST00000271651.8:c.236G= MANE Select	ENSP00000271651.3:p.Gly79=
NM_000396.3:c.236G=	NP_000387.1:p.Gly79=
ENST00000271651.7:c.236G=	ENSP00000271651.3:p.Gly79=
ENST00000443913.1:c.413G=	ENSP00000405083.1:p.Gly138=
ENST00000443913.2:c.413G=	ENSP00000405083.2:p.Gly138=
ENST00000480670.1:n.84-93G=
ENST00000480670.2:n.3305G=
ENST00000676680.1:c.236G=	ENSP00000503270.1:p.Gly79=
ENST00000676716.1:c.121-93G=	ENSP00000504737.1:n.121-93G=
ENST00000676751.1:c.236G=	ENSP00000502964.1:p.Gly79=
ENST00000676824.1:c.236G=	ENSP00000504176.1:p.Gly79=
ENST00000676966.1:c.236G=	ENSP00000503723.1:p.Gly79=
ENST00000676970.1:c.236G=	ENSP00000503832.1:p.Gly79=
ENST00000677330.1:n.2062G=
ENST00000677611.1:n.3G=
ENST00000677887.1:c.278G=	ENSP00000503876.1:p.Gly93=
ENST00000678275.1:c.*128G=	ENSP00000504796.1:n.*128G=
ENST00000678337.1:c.272G=	ENSP00000504759.1:p.Gly91=
ENST00000678725.1:n.1213G=
ENST00000679090.1:n.821G=
ENST00000679148.1:n.1577G=
ENST00000679171.1:n.2597G=
ENST00000679260.1:c.236G=	ENSP00000504534.1:p.Gly79=