Canonical Allele Identifier: CA2326525493
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785959_18785970delinsCCGTACTGTCCG , CM000681.2:g.18785959_18785970delinsCCGTACTGTCCG GRCh38
NC_000019.9:g.18896769_18896780delinsCCGTACTGTCCG , CM000681.1:g.18896769_18896780delinsCCGTACTGTCCG GRCh37
NC_000019.8:g.18757769_18757780delinsCCGTACTGTCCG NCBI36
NG_007070.1:g.10335_10346delinsCGGACAGTACGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1484_1489+6delinsCGGACAGTACGG
ENST00000222271.6:c.1484_1489+6delinsCGGACAGTACGG
ENST00000425807.1:c.1325_1330+6delinsCGGACAGTACGG
ENST00000542601.6:c.1385_1390+6delinsCGGACAGTACGG
NM_000095.2:c.1484_1489+6delinsCGGACAGTACGG
NM_000095.3:c.1484_1489+6delinsCGGACAGTACGG