Canonical Allele Identifier: CA2326524899
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784971C= , CM000681.2:g.18784971C= GRCh38
NC_000019.9:g.18895781C= , CM000681.1:g.18895781C= GRCh37
NC_000019.8:g.18756781C= NCBI36
NG_007070.1:g.11334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1839G= MANE Select ENSP00000222271.2:p.Met613=
ENST00000222271.6:c.1839G= ENSP00000222271.2:p.Met613=
ENST00000425807.1:c.1680G= ENSP00000403792.1:p.Met560=
ENST00000542601.6:c.1740G= ENSP00000439156.2:p.Met580=
NM_000095.2:c.1839G= NP_000086.2:p.Met613=
NM_000095.3:c.1839G= MANE Select NP_000086.2:p.Met613=