Canonical Allele Identifier: CA2479314229

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804178T= , CM000663.2:g.150804178T=	GRCh38
NC_000001.10:g.150776654T= , CM000663.1:g.150776654T=	GRCh37
NC_000001.9:g.149043278T=	NCBI36
NG_011848.1:g.9159A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.461A= MANE Select	ENSP00000271651.3:p.Lys154=
ENST00000443913.2:c.638A=	ENSP00000405083.2:p.Lys213=
ENST00000480670.2:n.3530A=
ENST00000676680.1:c.461A=	ENSP00000503270.1:p.Lys154=
ENST00000676716.1:c.338A=	ENSP00000504737.1:p.Lys113=
ENST00000676751.1:c.461A=	ENSP00000502964.1:p.Lys154=
ENST00000676824.1:c.461A=	ENSP00000504176.1:p.Lys154=
ENST00000676966.1:c.461A=	ENSP00000503723.1:p.Lys154=
ENST00000676970.1:c.461A=	ENSP00000503832.1:p.Lys154=
ENST00000677330.1:n.2287A=
ENST00000677611.1:n.313A=
ENST00000677887.1:c.503A=	ENSP00000503876.1:p.Lys168=
ENST00000678275.1:c.*353A=	ENSP00000504796.1:n.*353A=
ENST00000678337.1:c.497A=	ENSP00000504759.1:p.Lys166=
ENST00000678725.1:n.1438A=
ENST00000679090.1:n.1046A=
ENST00000679148.1:n.3423A=
ENST00000679171.1:n.2822A=
ENST00000679260.1:c.399+1683A=	ENSP00000504534.1:n.399+1683A=
ENST00000271651.7:c.461A=	ENSP00000271651.3:p.Lys154=
ENST00000443913.1:c.638A=	ENSP00000405083.1:p.Lys213=
ENST00000480670.1:n.301A=
NM_000396.3:c.461A=	NP_000387.1:p.Lys154=
NM_000396.4:c.461A= MANE Select	NP_000387.1:p.Lys154=