Canonical Allele Identifier: CA420699483

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776680C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804204C>A , CM000663.2:g.150804204C>A	GRCh38
NC_000001.10:g.150776680C>A , CM000663.1:g.150776680C>A	GRCh37
NC_000001.9:g.149043304C>A	NCBI36
NG_011848.1:g.9133G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.435G>T MANE Select	ENSP00000271651.3:p.Val145=
ENST00000443913.2:c.612G>T	ENSP00000405083.2:p.Val204=
ENST00000480670.2:n.3504G>T
ENST00000676680.1:c.435G>T	ENSP00000503270.1:p.Val145=
ENST00000676716.1:c.312G>T	ENSP00000504737.1:p.Val104=
ENST00000676751.1:c.435G>T	ENSP00000502964.1:p.Val145=
ENST00000676824.1:c.435G>T	ENSP00000504176.1:p.Val145=
ENST00000676966.1:c.435G>T	ENSP00000503723.1:p.Val145=
ENST00000676970.1:c.435G>T	ENSP00000503832.1:p.Val145=
ENST00000677330.1:n.2261G>T
ENST00000677611.1:n.287G>T
ENST00000677887.1:c.477G>T	ENSP00000503876.1:p.Val159=
ENST00000678275.1:c.*327G>T	ENSP00000504796.1:n.*327G>T
ENST00000678337.1:c.471G>T	ENSP00000504759.1:p.Val157=
ENST00000678725.1:n.1412G>T
ENST00000679090.1:n.1020G>T
ENST00000679148.1:n.3397G>T
ENST00000679171.1:n.2796G>T
ENST00000679260.1:c.399+1657G>T	ENSP00000504534.1:n.399+1657G>T
ENST00000271651.7:c.435G>T	ENSP00000271651.3:p.Val145=
ENST00000443913.1:c.612G>T	ENSP00000405083.1:p.Val204=
ENST00000480670.1:n.275G>T
NM_000396.3:c.435G>T	NP_000387.1:p.Val145=
NM_000396.4:c.435G>T MANE Select	NP_000387.1:p.Val145=