Canonical Allele Identifier: CA342336662
Gene: CTSK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150804176T>A , CM000663.2:g.150804176T>A GRCh38
NC_000001.10:g.150776652T>A , CM000663.1:g.150776652T>A GRCh37
NC_000001.9:g.149043276T>A NCBI36
NG_011848.1:g.9161A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271651.8:c.463A>T MANE Select ENSP00000271651.3:p.Lys155Ter
ENST00000443913.2:c.640A>T ENSP00000405083.2:p.Lys214Ter
ENST00000480670.2:n.3532A>T
ENST00000676680.1:c.463A>T ENSP00000503270.1:p.Lys155Ter
ENST00000676716.1:c.340A>T ENSP00000504737.1:p.Lys114Ter
ENST00000676751.1:c.463A>T ENSP00000502964.1:p.Lys155Ter
ENST00000676824.1:c.463A>T ENSP00000504176.1:p.Lys155Ter
ENST00000676966.1:c.463A>T ENSP00000503723.1:p.Lys155Ter
ENST00000676970.1:c.463A>T ENSP00000503832.1:p.Lys155Ter
ENST00000677330.1:n.2289A>T
ENST00000677611.1:n.315A>T
ENST00000677887.1:c.505A>T ENSP00000503876.1:p.Lys169Ter
ENST00000678275.1:c.*355A>T ENSP00000504796.1:n.*355A>T
ENST00000678337.1:c.499A>T ENSP00000504759.1:p.Lys167Ter
ENST00000678725.1:n.1440A>T
ENST00000679090.1:n.1048A>T
ENST00000679148.1:n.3425A>T
ENST00000679171.1:n.2824A>T
ENST00000679260.1:c.399+1685A>T ENSP00000504534.1:n.399+1685A>T
ENST00000271651.7:c.463A>T ENSP00000271651.3:p.Lys155Ter
ENST00000443913.1:c.640A>T ENSP00000405083.1:p.Lys214Ter
ENST00000480670.1:n.303A>T
NM_000396.3:c.463A>T NP_000387.1:p.Lys155Ter
NM_000396.4:c.463A>T MANE Select NP_000387.1:p.Lys155Ter