Canonical Allele Identifier: CA2326526463
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787521C= , CM000681.2:g.18787521C= GRCh38
NC_000019.9:g.18898330C= , CM000681.1:g.18898330C= GRCh37
NC_000019.8:g.18759330C= NCBI36
NG_007070.1:g.8785G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1105G= MANE Select ENSP00000222271.2:p.Asp369=
ENST00000222271.6:c.1105G= ENSP00000222271.2:p.Asp369=
ENST00000425807.1:c.946G= ENSP00000403792.1:p.Asp316=
ENST00000542601.6:c.1006G= ENSP00000439156.2:p.Asp336=
NM_000095.2:c.1105G= NP_000086.2:p.Asp369=
NM_000095.3:c.1105G= MANE Select NP_000086.2:p.Asp369=