Canonical Allele Identifier: CA420699362

Gene: CTSK

Linked Data

• dbSNP Id: rs1654040694
• MyVariant Identifiers: chr1:g.150776506A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804030A>G , CM000663.2:g.150804030A>G	GRCh38
NC_000001.10:g.150776506A>G , CM000663.1:g.150776506A>G	GRCh37
NC_000001.9:g.149043130A>G	NCBI36
NG_011848.1:g.9307T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.609T>C MANE Select	ENSP00000271651.3:p.Tyr203=
ENST00000443913.2:c.786T>C	ENSP00000405083.2:p.Tyr262=
ENST00000480670.2:n.3678T>C
ENST00000676680.1:c.609T>C	ENSP00000503270.1:p.Tyr203=
ENST00000676716.1:c.486T>C	ENSP00000504737.1:p.Tyr162=
ENST00000676751.1:c.609T>C	ENSP00000502964.1:p.Tyr203=
ENST00000676824.1:c.609T>C	ENSP00000504176.1:p.Tyr203=
ENST00000676966.1:c.609T>C	ENSP00000503723.1:p.Tyr203=
ENST00000676970.1:c.609T>C	ENSP00000503832.1:p.Tyr203=
ENST00000677330.1:n.2435T>C
ENST00000677611.1:n.461T>C
ENST00000677887.1:c.651T>C	ENSP00000503876.1:p.Tyr217=
ENST00000678275.1:c.*501T>C	ENSP00000504796.1:n.*501T>C
ENST00000678337.1:c.645T>C	ENSP00000504759.1:p.Tyr215=
ENST00000678725.1:n.1586T>C
ENST00000679090.1:n.1194T>C
ENST00000679148.1:n.3571T>C
ENST00000679171.1:n.2970T>C
ENST00000679260.1:c.399+1831T>C	ENSP00000504534.1:n.399+1831T>C
ENST00000271651.7:c.609T>C	ENSP00000271651.3:p.Tyr203=
ENST00000480670.1:n.449T>C
NM_000396.3:c.609T>C	NP_000387.1:p.Tyr203=
NM_000396.4:c.609T>C MANE Select	NP_000387.1:p.Tyr203=