Canonical Allele Identifier: CA342337526
Gene: CTSK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150806688T>A , CM000663.2:g.150806688T>A GRCh38
NC_000001.10:g.150779164T>A , CM000663.1:g.150779164T>A GRCh37
NC_000001.9:g.149045788T>A NCBI36
NG_011848.1:g.6649A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000271651.8:c.118A>T MANE Select ENSP00000271651.3:p.Lys40Ter
ENST00000443913.2:c.295A>T ENSP00000405083.2:p.Lys99Ter
ENST00000480670.2:n.2726A>T
ENST00000676680.1:c.118A>T ENSP00000503270.1:p.Lys40Ter
ENST00000676716.1:c.118A>T ENSP00000504737.1:p.Lys40Ter
ENST00000676751.1:c.118A>T ENSP00000502964.1:p.Lys40Ter
ENST00000676824.1:c.118A>T ENSP00000504176.1:p.Lys40Ter
ENST00000676966.1:c.118A>T ENSP00000503723.1:p.Lys40Ter
ENST00000676970.1:c.118A>T ENSP00000503832.1:p.Lys40Ter
ENST00000677330.1:n.1483A>T
ENST00000677887.1:c.160A>T ENSP00000503876.1:p.Lys54Ter
ENST00000678275.1:c.118A>T ENSP00000504796.1:p.Lys40Ter
ENST00000678337.1:c.154A>T ENSP00000504759.1:p.Lys52Ter
ENST00000678725.1:n.1095A>T
ENST00000679090.1:n.242A>T
ENST00000679148.1:n.998A>T
ENST00000679171.1:n.2018A>T
ENST00000679260.1:c.118A>T ENSP00000504534.1:p.Lys40Ter
ENST00000271651.7:c.118A>T ENSP00000271651.3:p.Lys40Ter
ENST00000443913.1:c.295A>T ENSP00000405083.1:p.Lys99Ter
ENST00000480670.1:n.81A>T
NM_000396.3:c.118A>T NP_000387.1:p.Lys40Ter
NM_000396.4:c.118A>T MANE Select NP_000387.1:p.Lys40Ter