Canonical Allele Identifier: CA404884319
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786009T>C , CM000681.2:g.18786009T>C GRCh38
NC_000019.9:g.18896819T>C , CM000681.1:g.18896819T>C GRCh37
NC_000019.8:g.18757819T>C NCBI36
NG_007070.1:g.10296A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1445A>G MANE Select ENSP00000222271.2:p.Asp482Gly
ENST00000222271.6:c.1445A>G ENSP00000222271.2:p.Asp482Gly
ENST00000425807.1:c.1286A>G ENSP00000403792.1:p.Asp429Gly
ENST00000542601.6:c.1346A>G ENSP00000439156.2:p.Asp449Gly
NM_000095.2:c.1445A>G NP_000086.2:p.Asp482Gly
NM_000095.3:c.1445A>G MANE Select NP_000086.2:p.Asp482Gly