Canonical Allele Identifier: CA2583621944
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785945_18785946insC , CM000681.2:g.18785945_18785946insC GRCh38
NC_000019.9:g.18896755_18896756insC , CM000681.1:g.18896755_18896756insC GRCh37
NC_000019.8:g.18757755_18757756insC NCBI36
NG_007070.1:g.10359_10360insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1489+19_1489+20insG MANE Select ENSP00000222271.2:n.1489+19_1489+20insG
ENST00000222271.6:c.1489+19_1489+20insG ENSP00000222271.2:n.1489+19_1489+20insG
ENST00000425807.1:c.1330+19_1330+20insG ENSP00000403792.1:n.1330+19_1330+20insG
ENST00000542601.6:c.1390+19_1390+20insG ENSP00000439156.2:n.1390+19_1390+20insG
NM_000095.2:c.1489+19_1489+20insG NP_000086.2:n.1489+19_1489+20insG
NM_000095.3:c.1489+19_1489+20insG MANE Select NP_000086.2:n.1489+19_1489+20insG