Canonical Allele Identifier: CA342336820

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150805860C>T , CM000663.2:g.150805860C>T	GRCh38
NC_000001.10:g.150778336C>T , CM000663.1:g.150778336C>T	GRCh37
NC_000001.9:g.149044960C>T	NCBI36
NG_011848.1:g.7477G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000396.4:c.399+1G>A MANE Select	NP_000387.1:n.399+1G>A
ENST00000271651.8:c.399+1G>A MANE Select	ENSP00000271651.3:n.399+1G>A
NM_000396.3:c.399+1G>A	NP_000387.1:n.399+1G>A
ENST00000271651.7:c.399+1G>A	ENSP00000271651.3:n.399+1G>A
ENST00000443913.1:c.576+1G>A	ENSP00000405083.1:n.576+1G>A
ENST00000443913.2:c.576+1G>A	ENSP00000405083.2:n.576+1G>A
ENST00000480670.1:n.239+1G>A
ENST00000480670.2:n.3468+1G>A
ENST00000676680.1:c.399+1G>A	ENSP00000503270.1:n.399+1G>A
ENST00000676716.1:c.276+1G>A	ENSP00000504737.1:n.276+1G>A
ENST00000676751.1:c.399+1G>A	ENSP00000502964.1:n.399+1G>A
ENST00000676824.1:c.399+1G>A	ENSP00000504176.1:n.399+1G>A
ENST00000676966.1:c.399+1G>A	ENSP00000503723.1:n.399+1G>A
ENST00000676970.1:c.399+1G>A	ENSP00000503832.1:n.399+1G>A
ENST00000677330.1:n.2225+1G>A
ENST00000677611.1:n.251+1G>A
ENST00000677887.1:c.441+1G>A	ENSP00000503876.1:n.441+1G>A
ENST00000678275.1:c.*291+1G>A	ENSP00000504796.1:n.*291+1G>A
ENST00000678337.1:c.435+1G>A	ENSP00000504759.1:n.435+1G>A
ENST00000678725.1:n.1376+1G>A
ENST00000679090.1:n.984+1G>A
ENST00000679148.1:n.1741G>A
ENST00000679171.1:n.2760+1G>A
ENST00000679260.1:c.399+1G>A	ENSP00000504534.1:n.399+1G>A