Canonical Allele Identifier: CA2326525505
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785976T= , CM000681.2:g.18785976T= GRCh38
NC_000019.9:g.18896786T= , CM000681.1:g.18896786T= GRCh37
NC_000019.8:g.18757786T= NCBI36
NG_007070.1:g.10329A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1478A= MANE Select ENSP00000222271.2:p.Glu493=
ENST00000222271.6:c.1478A= ENSP00000222271.2:p.Glu493=
ENST00000425807.1:c.1319A= ENSP00000403792.1:p.Glu440=
ENST00000542601.6:c.1379A= ENSP00000439156.2:p.Glu460=
NM_000095.2:c.1478A= NP_000086.2:p.Glu493=
NM_000095.3:c.1478A= MANE Select NP_000086.2:p.Glu493=