Canonical Allele Identifier: CA994237986
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs2055181084
gnomAD v3: 19-18787902-C-CTTTT
gnomAD v4: 19-18787902-C-CTTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787905_18787906insTTTT , CM000681.2:g.18787905_18787906insTTTT GRCh38
NC_000019.9:g.18898714_18898715insTTTT , CM000681.1:g.18898714_18898715insTTTT GRCh37
NC_000019.8:g.18759714_18759715insTTTT NCBI36
NG_007070.1:g.8403_8404insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-253_976-252insAAAA MANE Select ENSP00000222271.2:n.976-253_976-252insAAAA
ENST00000222271.6:c.976-253_976-252insAAAA ENSP00000222271.2:n.976-253_976-252insAAAA
ENST00000425807.1:c.817-253_817-252insAAAA ENSP00000403792.1:n.817-253_817-252insAAAA
ENST00000542601.6:c.877-253_877-252insAAAA ENSP00000439156.2:n.877-253_877-252insAAAA
NM_000095.2:c.976-253_976-252insAAAA NP_000086.2:n.976-253_976-252insAAAA
NM_000095.3:c.976-253_976-252insAAAA MANE Select NP_000086.2:n.976-253_976-252insAAAA
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Search 100 bp 3'