Canonical Allele Identifier: CA506053133
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18898655_18898656insTCTTTC (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787847_18787848insCTTTCT , CM000681.2:g.18787847_18787848insCTTTCT GRCh38
NC_000019.9:g.18898656_18898657insCTTTCT , CM000681.1:g.18898656_18898657insCTTTCT GRCh37
NC_000019.8:g.18759656_18759657insCTTTCT NCBI36
NG_007070.1:g.8459_8460insGAAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-197_976-196insGAAAGA MANE Select ENSP00000222271.2:n.976-197_976-196insGAAAGA
ENST00000222271.6:c.976-197_976-196insGAAAGA ENSP00000222271.2:n.976-197_976-196insGAAAGA
ENST00000425807.1:c.817-197_817-196insGAAAGA ENSP00000403792.1:n.817-197_817-196insGAAAGA
ENST00000542601.6:c.877-197_877-196insGAAAGA ENSP00000439156.2:n.877-197_877-196insGAAAGA
NM_000095.2:c.976-197_976-196insGAAAGA NP_000086.2:n.976-197_976-196insGAAAGA
NM_000095.3:c.976-197_976-196insGAAAGA MANE Select NP_000086.2:n.976-197_976-196insGAAAGA
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