Canonical Allele Identifier: CA342336657
Gene: CTSK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804174T>A , CM000663.2:g.150804174T>A GRCh38
NC_000001.10:g.150776650T>A , CM000663.1:g.150776650T>A GRCh37
NC_000001.9:g.149043274T>A NCBI36
NG_011848.1:g.9163A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.465A>T MANE Select ENSP00000271651.3:p.Lys155Asn
ENST00000443913.2:c.642A>T ENSP00000405083.2:p.Lys214Asn
ENST00000480670.2:n.3534A>T
ENST00000676680.1:c.465A>T ENSP00000503270.1:p.Lys155Asn
ENST00000676716.1:c.342A>T ENSP00000504737.1:p.Lys114Asn
ENST00000676751.1:c.465A>T ENSP00000502964.1:p.Lys155Asn
ENST00000676824.1:c.465A>T ENSP00000504176.1:p.Lys155Asn
ENST00000676966.1:c.465A>T ENSP00000503723.1:p.Lys155Asn
ENST00000676970.1:c.465A>T ENSP00000503832.1:p.Lys155Asn
ENST00000677330.1:n.2291A>T
ENST00000677611.1:n.317A>T
ENST00000677887.1:c.507A>T ENSP00000503876.1:p.Lys169Asn
ENST00000678275.1:c.*357A>T ENSP00000504796.1:n.*357A>T
ENST00000678337.1:c.501A>T ENSP00000504759.1:p.Lys167Asn
ENST00000678725.1:n.1442A>T
ENST00000679090.1:n.1050A>T
ENST00000679148.1:n.3427A>T
ENST00000679171.1:n.2826A>T
ENST00000679260.1:c.399+1687A>T ENSP00000504534.1:n.399+1687A>T
ENST00000271651.7:c.465A>T ENSP00000271651.3:p.Lys155Asn
ENST00000443913.1:c.642A>T ENSP00000405083.1:p.Lys214Asn
ENST00000480670.1:n.305A>T
NM_000396.3:c.465A>T NP_000387.1:p.Lys155Asn
NM_000396.4:c.465A>T MANE Select NP_000387.1:p.Lys155Asn