Canonical Allele Identifier: CA306255220
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1045068010

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786009del , CM000681.2:g.18786009del GRCh38
NC_000019.9:g.18896819del , CM000681.1:g.18896819del GRCh37
NC_000019.8:g.18757819del NCBI36
NG_007070.1:g.10296del

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1445del MANE Select ENSP00000222271.2:p.Asp482AlafsTer?
ENST00000222271.6:c.1445del ENSP00000222271.2:p.Asp482AlafsTer?
ENST00000425807.1:c.1286del ENSP00000403792.1:p.Asp429AlafsTer?
ENST00000542601.6:c.1346del ENSP00000439156.2:p.Asp449AlafsTer?
NM_000095.2:c.1445del NP_000086.2:p.Asp482AlafsTer?
NM_000095.3:c.1445del MANE Select NP_000086.2:p.Asp482AlafsTer?