Canonical Allele Identifier: CA342336726

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776681A>G (hg19) ; chr1:g.150804205A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804205A>G , CM000663.2:g.150804205A>G	GRCh38
NC_000001.10:g.150776681A>G , CM000663.1:g.150776681A>G	GRCh37
NC_000001.9:g.149043305A>G	NCBI36
NG_011848.1:g.9132T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.434T>C MANE Select	ENSP00000271651.3:p.Val145Ala
ENST00000443913.2:c.611T>C	ENSP00000405083.2:p.Val204Ala
ENST00000480670.2:n.3503T>C
ENST00000676680.1:c.434T>C	ENSP00000503270.1:p.Val145Ala
ENST00000676716.1:c.311T>C	ENSP00000504737.1:p.Val104Ala
ENST00000676751.1:c.434T>C	ENSP00000502964.1:p.Val145Ala
ENST00000676824.1:c.434T>C	ENSP00000504176.1:p.Val145Ala
ENST00000676966.1:c.434T>C	ENSP00000503723.1:p.Val145Ala
ENST00000676970.1:c.434T>C	ENSP00000503832.1:p.Val145Ala
ENST00000677330.1:n.2260T>C
ENST00000677611.1:n.286T>C
ENST00000677887.1:c.476T>C	ENSP00000503876.1:p.Val159Ala
ENST00000678275.1:c.*326T>C	ENSP00000504796.1:n.*326T>C
ENST00000678337.1:c.470T>C	ENSP00000504759.1:p.Val157Ala
ENST00000678725.1:n.1411T>C
ENST00000679090.1:n.1019T>C
ENST00000679148.1:n.3396T>C
ENST00000679171.1:n.2795T>C
ENST00000679260.1:c.399+1656T>C	ENSP00000504534.1:n.399+1656T>C
ENST00000271651.7:c.434T>C	ENSP00000271651.3:p.Val145Ala
ENST00000443913.1:c.611T>C	ENSP00000405083.1:p.Val204Ala
ENST00000480670.1:n.274T>C
NM_000396.3:c.434T>C	NP_000387.1:p.Val145Ala
NM_000396.4:c.434T>C MANE Select	NP_000387.1:p.Val145Ala