Canonical Allele Identifier: CA404884238
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785989T>C , CM000681.2:g.18785989T>C GRCh38
NC_000019.9:g.18896799T>C , CM000681.1:g.18896799T>C GRCh37
NC_000019.8:g.18757799T>C NCBI36
NG_007070.1:g.10316A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1465A>G MANE Select ENSP00000222271.2:p.Asn489Asp
ENST00000222271.6:c.1465A>G ENSP00000222271.2:p.Asn489Asp
ENST00000425807.1:c.1306A>G ENSP00000403792.1:p.Asn436Asp
ENST00000542601.6:c.1366A>G ENSP00000439156.2:p.Asn456Asp
NM_000095.2:c.1465A>G NP_000086.2:p.Asn489Asp
NM_000095.3:c.1465A>G MANE Select NP_000086.2:p.Asn489Asp