Canonical Allele Identifier: CA342336576

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776612A>C (hg19) ; chr1:g.150804136A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804136A>C , CM000663.2:g.150804136A>C	GRCh38
NC_000001.10:g.150776612A>C , CM000663.1:g.150776612A>C	GRCh37
NC_000001.9:g.149043236A>C	NCBI36
NG_011848.1:g.9201T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.503T>G MANE Select	ENSP00000271651.3:p.Val168Gly
ENST00000443913.2:c.680T>G	ENSP00000405083.2:p.Val227Gly
ENST00000480670.2:n.3572T>G
ENST00000676680.1:c.503T>G	ENSP00000503270.1:p.Val168Gly
ENST00000676716.1:c.380T>G	ENSP00000504737.1:p.Val127Gly
ENST00000676751.1:c.503T>G	ENSP00000502964.1:p.Val168Gly
ENST00000676824.1:c.503T>G	ENSP00000504176.1:p.Val168Gly
ENST00000676966.1:c.503T>G	ENSP00000503723.1:p.Val168Gly
ENST00000676970.1:c.503T>G	ENSP00000503832.1:p.Val168Gly
ENST00000677330.1:n.2329T>G
ENST00000677611.1:n.355T>G
ENST00000677887.1:c.545T>G	ENSP00000503876.1:p.Val182Gly
ENST00000678275.1:c.*395T>G	ENSP00000504796.1:n.*395T>G
ENST00000678337.1:c.539T>G	ENSP00000504759.1:p.Val180Gly
ENST00000678725.1:n.1480T>G
ENST00000679090.1:n.1088T>G
ENST00000679148.1:n.3465T>G
ENST00000679171.1:n.2864T>G
ENST00000679260.1:c.399+1725T>G	ENSP00000504534.1:n.399+1725T>G
ENST00000271651.7:c.503T>G	ENSP00000271651.3:p.Val168Gly
ENST00000443913.1:c.680T>G	ENSP00000405083.1:p.Val227Gly
ENST00000480670.1:n.343T>G
NM_000396.3:c.503T>G	NP_000387.1:p.Val168Gly
NM_000396.4:c.503T>G MANE Select	NP_000387.1:p.Val168Gly