Canonical Allele Identifier: CA2583621927
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785930_18785933dup , CM000681.2:g.18785930_18785933dup GRCh38
NC_000019.9:g.18896740_18896743dup , CM000681.1:g.18896740_18896743dup GRCh37
NC_000019.8:g.18757740_18757743dup NCBI36
NG_007070.1:g.10372_10375dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1489+32_1489+35dup MANE Select ENSP00000222271.2:n.1489+32_1489+35dup
ENST00000222271.6:c.1489+32_1489+35dup ENSP00000222271.2:n.1489+32_1489+35dup
ENST00000425807.1:c.1330+32_1330+35dup ENSP00000403792.1:n.1330+32_1330+35dup
ENST00000542601.6:c.1390+32_1390+35dup ENSP00000439156.2:n.1390+32_1390+35dup
NM_000095.2:c.1489+32_1489+35dup NP_000086.2:n.1489+32_1489+35dup
NM_000095.3:c.1489+32_1489+35dup MANE Select NP_000086.2:n.1489+32_1489+35dup