Canonical Allele Identifier: CA342337774
Community Standard Title: NM_000396.4(CTSK):c.5G>A (p.Trp2Ter)
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150806801C>T , CM000663.2:g.150806801C>T GRCh38
NC_000001.10:g.150779277C>T , CM000663.1:g.150779277C>T GRCh37
NC_000001.9:g.149045901C>T NCBI36
NG_011848.1:g.6536G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000396.4:c.5G>A MANE Select NP_000387.1:p.Trp2Ter
ENST00000271651.8:c.5G>A MANE Select ENSP00000271651.3:p.Trp2Ter
NM_000396.3:c.5G>A NP_000387.1:p.Trp2Ter
ENST00000271651.7:c.5G>A ENSP00000271651.3:p.Trp2Ter
ENST00000443913.1:c.182G>A ENSP00000405083.1:p.Trp61Ter
ENST00000443913.2:c.182G>A ENSP00000405083.2:p.Trp61Ter
ENST00000480670.2:n.2613G>A
ENST00000676680.1:c.5G>A ENSP00000503270.1:p.Trp2Ter
ENST00000676716.1:c.5G>A ENSP00000504737.1:p.Trp2Ter
ENST00000676751.1:c.5G>A ENSP00000502964.1:p.Trp2Ter
ENST00000676824.1:c.5G>A ENSP00000504176.1:p.Trp2Ter
ENST00000676966.1:c.5G>A ENSP00000503723.1:p.Trp2Ter
ENST00000676970.1:c.5G>A ENSP00000503832.1:p.Trp2Ter
ENST00000677330.1:n.1370G>A
ENST00000677887.1:c.47G>A ENSP00000503876.1:p.Trp16Ter
ENST00000678275.1:c.5G>A ENSP00000504796.1:p.Trp2Ter
ENST00000678337.1:c.41G>A ENSP00000504759.1:p.Trp14Ter
ENST00000678725.1:n.982G>A
ENST00000679090.1:n.129G>A
ENST00000679148.1:n.885G>A
ENST00000679171.1:n.1905G>A
ENST00000679260.1:c.5G>A ENSP00000504534.1:p.Trp2Ter