Canonical Allele Identifier: CA342336589

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776618T>A (hg19) ; chr1:g.150804142T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804142T>A , CM000663.2:g.150804142T>A	GRCh38
NC_000001.10:g.150776618T>A , CM000663.1:g.150776618T>A	GRCh37
NC_000001.9:g.149043242T>A	NCBI36
NG_011848.1:g.9195A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.497A>T MANE Select	ENSP00000271651.3:p.Asn166Ile
ENST00000443913.2:c.674A>T	ENSP00000405083.2:p.Asn225Ile
ENST00000480670.2:n.3566A>T
ENST00000676680.1:c.497A>T	ENSP00000503270.1:p.Asn166Ile
ENST00000676716.1:c.374A>T	ENSP00000504737.1:p.Asn125Ile
ENST00000676751.1:c.497A>T	ENSP00000502964.1:p.Asn166Ile
ENST00000676824.1:c.497A>T	ENSP00000504176.1:p.Asn166Ile
ENST00000676966.1:c.497A>T	ENSP00000503723.1:p.Asn166Ile
ENST00000676970.1:c.497A>T	ENSP00000503832.1:p.Asn166Ile
ENST00000677330.1:n.2323A>T
ENST00000677611.1:n.349A>T
ENST00000677887.1:c.539A>T	ENSP00000503876.1:p.Asn180Ile
ENST00000678275.1:c.*389A>T	ENSP00000504796.1:n.*389A>T
ENST00000678337.1:c.533A>T	ENSP00000504759.1:p.Asn178Ile
ENST00000678725.1:n.1474A>T
ENST00000679090.1:n.1082A>T
ENST00000679148.1:n.3459A>T
ENST00000679171.1:n.2858A>T
ENST00000679260.1:c.399+1719A>T	ENSP00000504534.1:n.399+1719A>T
ENST00000271651.7:c.497A>T	ENSP00000271651.3:p.Asn166Ile
ENST00000443913.1:c.674A>T	ENSP00000405083.1:p.Asn225Ile
ENST00000480670.1:n.337A>T
NM_000396.3:c.497A>T	NP_000387.1:p.Asn166Ile
NM_000396.4:c.497A>T MANE Select	NP_000387.1:p.Asn166Ile