Canonical Allele Identifier: CA118672
Gene: CTSC HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7289
ClinVar RCV Id: RCV000007712
dbSNP Id: rs104894206

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88309176G>A , CM000673.2:g.88309176G>A GRCh38
NC_000011.9:g.88042344G>A , CM000673.1:g.88042344G>A GRCh37
NC_000011.8:g.87681992G>A NCBI36
NG_007952.1:g.33598C>T , LRG_50:g.33598C>T

Transcript Alleles

HGVS Amino-acid change
NM_001814.4:c.628C>T , LRG_50t1:c.628C>T NP_001805.3:p.Arg210Ter
NM_001814.5:c.628C>T VV NP_001805.3:p.Arg210Ter
NM_001814.6:c.628C>T VV MANE Preferred NP_001805.4:p.Arg210Ter
ENST00000227266.9:c.628C>T ENSP00000227266.4:p.Arg210Ter
ENST00000527018.5:n.498C>T