Canonical Allele Identifier: CA2326526457
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787507G= , CM000681.2:g.18787507G= GRCh38
NC_000019.9:g.18898316G= , CM000681.1:g.18898316G= GRCh37
NC_000019.8:g.18759316G= NCBI36
NG_007070.1:g.8799C=

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1119C= MANE Select ENSP00000222271.2:p.Asp373=
ENST00000222271.6:c.1119C= ENSP00000222271.2:p.Asp373=
ENST00000425807.1:c.960C= ENSP00000403792.1:p.Asp320=
ENST00000542601.6:c.1020C= ENSP00000439156.2:p.Asp340=
NM_000095.2:c.1119C= NP_000086.2:p.Asp373=
NM_000095.3:c.1119C= MANE Select NP_000086.2:p.Asp373=