Canonical Allele Identifier: CA2326526499
Gene: COMP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787872_18787886delinsTTCTTTCTTTCTTTC , CM000681.2:g.18787872_18787886delinsTTCTTTCTTTCTTTC GRCh38
NC_000019.9:g.18898681_18898695delinsTTCTTTCTTTCTTTC , CM000681.1:g.18898681_18898695delinsTTCTTTCTTTCTTTC GRCh37
NC_000019.8:g.18759681_18759695delinsTTCTTTCTTTCTTTC NCBI36
NG_007070.1:g.8420_8434delinsGAAAGAAAGAAAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-236_976-222delinsGAAAGAAAGAAAGAA MANE Select ENSP00000222271.2:n.976-236_976-222delinsGAAAGAAAGAAAGAA
ENST00000222271.6:c.976-236_976-222delinsGAAAGAAAGAAAGAA ENSP00000222271.2:n.976-236_976-222delinsGAAAGAAAGAAAGAA
ENST00000425807.1:c.817-236_817-222delinsGAAAGAAAGAAAGAA ENSP00000403792.1:n.817-236_817-222delinsGAAAGAAAGAAAGAA
ENST00000542601.6:c.877-236_877-222delinsGAAAGAAAGAAAGAA ENSP00000439156.2:n.877-236_877-222delinsGAAAGAAAGAAAGAA
NM_000095.2:c.976-236_976-222delinsGAAAGAAAGAAAGAA NP_000086.2:n.976-236_976-222delinsGAAAGAAAGAAAGAA
NM_000095.3:c.976-236_976-222delinsGAAAGAAAGAAAGAA MANE Select NP_000086.2:n.976-236_976-222delinsGAAAGAAAGAAAGAA
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