Canonical Allele Identifier: CA404885081
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786113G>T , CM000681.2:g.18786113G>T GRCh38
NC_000019.9:g.18896923G>T , CM000681.1:g.18896923G>T GRCh37
NC_000019.8:g.18757923G>T NCBI36
NG_007070.1:g.10192C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1341C>A MANE Select ENSP00000222271.2:p.Asn447Lys
ENST00000222271.6:c.1341C>A ENSP00000222271.2:p.Asn447Lys
ENST00000425807.1:c.1182C>A ENSP00000403792.1:p.Asn394Lys
ENST00000542601.6:c.1242C>A ENSP00000439156.2:p.Asn414Lys
NM_000095.2:c.1341C>A NP_000086.2:p.Asn447Lys
NM_000095.3:c.1341C>A MANE Select NP_000086.2:p.Asn447Lys