Canonical Allele Identifier: CA404884832
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786078G>C , CM000681.2:g.18786078G>C GRCh38
NC_000019.9:g.18896888G>C , CM000681.1:g.18896888G>C GRCh37
NC_000019.8:g.18757888G>C NCBI36
NG_007070.1:g.10227C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1376C>G MANE Select ENSP00000222271.2:p.Ser459Ter
ENST00000222271.6:c.1376C>G ENSP00000222271.2:p.Ser459Ter
ENST00000425807.1:c.1217C>G ENSP00000403792.1:p.Ser406Ter
ENST00000542601.6:c.1277C>G ENSP00000439156.2:p.Ser426Ter
NM_000095.2:c.1376C>G NP_000086.2:p.Ser459Ter
NM_000095.3:c.1376C>G MANE Select NP_000086.2:p.Ser459Ter