Canonical Allele Identifier: CA16040662
Gene: CTSK HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 370816
ClinVar RCV Id: RCV000412289
dbSNP Id: rs1057516790

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150806758del , CM000663.2:g.150806758del GRCh38
NC_000001.10:g.150779234del , CM000663.1:g.150779234del GRCh37
NC_000001.9:g.149045858del NCBI36
NG_011848.1:g.6579del

Transcript Alleles

HGVS Amino-acid change
NM_000396.3:c.48del VV NP_000387.1:p.Tyr17ThrfsTer?
NM_000396.4:c.48del VV MANE Preferred NP_000387.1:p.Tyr17ThrfsTer?
ENST00000271651.7:c.48del ENSP00000271651.3:p.Tyr17ThrfsTer?
ENST00000443913.1:c.225del ENSP00000405083.1:p.Tyr76ThrfsTer?
ENST00000480670.1:n.11del