Canonical Allele Identifier: CA420699489

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776689A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804213A>G , CM000663.2:g.150804213A>G	GRCh38
NC_000001.10:g.150776689A>G , CM000663.1:g.150776689A>G	GRCh37
NC_000001.9:g.149043313A>G	NCBI36
NG_011848.1:g.9124T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.426T>C MANE Select	ENSP00000271651.3:p.Phe142=
ENST00000443913.2:c.603T>C	ENSP00000405083.2:p.Phe201=
ENST00000480670.2:n.3495T>C
ENST00000676680.1:c.426T>C	ENSP00000503270.1:p.Phe142=
ENST00000676716.1:c.303T>C	ENSP00000504737.1:p.Phe101=
ENST00000676751.1:c.426T>C	ENSP00000502964.1:p.Phe142=
ENST00000676824.1:c.426T>C	ENSP00000504176.1:p.Phe142=
ENST00000676966.1:c.426T>C	ENSP00000503723.1:p.Phe142=
ENST00000676970.1:c.426T>C	ENSP00000503832.1:p.Phe142=
ENST00000677330.1:n.2252T>C
ENST00000677611.1:n.278T>C
ENST00000677887.1:c.468T>C	ENSP00000503876.1:p.Phe156=
ENST00000678275.1:c.*318T>C	ENSP00000504796.1:n.*318T>C
ENST00000678337.1:c.462T>C	ENSP00000504759.1:p.Phe154=
ENST00000678725.1:n.1403T>C
ENST00000679090.1:n.1011T>C
ENST00000679148.1:n.3388T>C
ENST00000679171.1:n.2787T>C
ENST00000679260.1:c.399+1648T>C	ENSP00000504534.1:n.399+1648T>C
ENST00000271651.7:c.426T>C	ENSP00000271651.3:p.Phe142=
ENST00000443913.1:c.603T>C	ENSP00000405083.1:p.Phe201=
ENST00000480670.1:n.266T>C
NM_000396.3:c.426T>C	NP_000387.1:p.Phe142=
NM_000396.4:c.426T>C MANE Select	NP_000387.1:p.Phe142=