Canonical Allele Identifier: CA2326524015
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18783131A= , CM000681.2:g.18783131A= GRCh38
NC_000019.9:g.18893941A= , CM000681.1:g.18893941A= GRCh37
NC_000019.8:g.18754941A= NCBI36
NG_007070.1:g.13174T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.2150T= MANE Select ENSP00000222271.2:p.Met717=
ENST00000222271.6:c.2150T= ENSP00000222271.2:p.Met717=
ENST00000425807.1:c.1991T= ENSP00000403792.1:p.Met664=
ENST00000542601.6:c.2051T= ENSP00000439156.2:p.Met684=
NM_000095.2:c.2150T= NP_000086.2:p.Met717=
NM_000095.3:c.2150T= MANE Select NP_000086.2:p.Met717=