Canonical Allele Identifier: CA2535387977
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787889_18787890insTTTTCTTTTTTT , CM000681.2:g.18787889_18787890insTTTTCTTTTTTT GRCh38
NC_000019.9:g.18898698_18898699insTTTTCTTTTTTT , CM000681.1:g.18898698_18898699insTTTTCTTTTTTT GRCh37
NC_000019.8:g.18759698_18759699insTTTTCTTTTTTT NCBI36
NG_007070.1:g.8419_8420insAAAAGAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-237_976-236insAAAAGAAAAAAA MANE Select ENSP00000222271.2:n.976-237_976-236insAAAAGAAAAAAA
ENST00000222271.6:c.976-237_976-236insAAAAGAAAAAAA ENSP00000222271.2:n.976-237_976-236insAAAAGAAAAAAA
ENST00000425807.1:c.817-237_817-236insAAAAGAAAAAAA ENSP00000403792.1:n.817-237_817-236insAAAAGAAAAAAA
ENST00000542601.6:c.877-237_877-236insAAAAGAAAAAAA ENSP00000439156.2:n.877-237_877-236insAAAAGAAAAAAA
NM_000095.2:c.976-237_976-236insAAAAGAAAAAAA NP_000086.2:n.976-237_976-236insAAAAGAAAAAAA
NM_000095.3:c.976-237_976-236insAAAAGAAAAAAA MANE Select NP_000086.2:n.976-237_976-236insAAAAGAAAAAAA
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