Canonical Allele Identifier: CA2526512682
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787908_18787922del , CM000681.2:g.18787908_18787922del GRCh38
NC_000019.9:g.18898717_18898731del , CM000681.1:g.18898717_18898731del GRCh37
NC_000019.8:g.18759717_18759731del NCBI36
NG_007070.1:g.8385_8399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-271_976-257del MANE Select ENSP00000222271.2:n.976-271_976-257del
ENST00000222271.6:c.976-271_976-257del ENSP00000222271.2:n.976-271_976-257del
ENST00000425807.1:c.817-271_817-257del ENSP00000403792.1:n.817-271_817-257del
ENST00000542601.6:c.877-271_877-257del ENSP00000439156.2:n.877-271_877-257del
NM_000095.2:c.976-271_976-257del NP_000086.2:n.976-271_976-257del
NM_000095.3:c.976-271_976-257del MANE Select NP_000086.2:n.976-271_976-257del
Search 100 bp 5'
Search 100 bp 3'