Canonical Allele Identifier: CA342336672
Gene: CTSK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804180C>A , CM000663.2:g.150804180C>A GRCh38
NC_000001.10:g.150776656C>A , CM000663.1:g.150776656C>A GRCh37
NC_000001.9:g.149043280C>A NCBI36
NG_011848.1:g.9157G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.459G>T MANE Select ENSP00000271651.3:p.Lys153Asn
ENST00000443913.2:c.636G>T ENSP00000405083.2:p.Lys212Asn
ENST00000480670.2:n.3528G>T
ENST00000676680.1:c.459G>T ENSP00000503270.1:p.Lys153Asn
ENST00000676716.1:c.336G>T ENSP00000504737.1:p.Lys112Asn
ENST00000676751.1:c.459G>T ENSP00000502964.1:p.Lys153Asn
ENST00000676824.1:c.459G>T ENSP00000504176.1:p.Lys153Asn
ENST00000676966.1:c.459G>T ENSP00000503723.1:p.Lys153Asn
ENST00000676970.1:c.459G>T ENSP00000503832.1:p.Lys153Asn
ENST00000677330.1:n.2285G>T
ENST00000677611.1:n.311G>T
ENST00000677887.1:c.501G>T ENSP00000503876.1:p.Lys167Asn
ENST00000678275.1:c.*351G>T ENSP00000504796.1:n.*351G>T
ENST00000678337.1:c.495G>T ENSP00000504759.1:p.Lys165Asn
ENST00000678725.1:n.1436G>T
ENST00000679090.1:n.1044G>T
ENST00000679148.1:n.3421G>T
ENST00000679171.1:n.2820G>T
ENST00000679260.1:c.399+1681G>T ENSP00000504534.1:n.399+1681G>T
ENST00000271651.7:c.459G>T ENSP00000271651.3:p.Lys153Asn
ENST00000443913.1:c.636G>T ENSP00000405083.1:p.Lys212Asn
ENST00000480670.1:n.299G>T
NM_000396.3:c.459G>T NP_000387.1:p.Lys153Asn
NM_000396.4:c.459G>T MANE Select NP_000387.1:p.Lys153Asn