Canonical Allele Identifier: CA994238055
Gene: COMP HGNC NCBI

Linked Data

gnomAD v3: 19-18787914-C-CTTT
gnomAD v4: 19-18787914-C-CTTT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787920_18787922dup , CM000681.2:g.18787920_18787922dup GRCh38
NC_000019.9:g.18898729_18898731dup , CM000681.1:g.18898729_18898731dup GRCh37
NC_000019.8:g.18759729_18759731dup NCBI36
NG_007070.1:g.8389_8391dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-267_976-265dup MANE Select ENSP00000222271.2:n.976-267_976-265dup
ENST00000222271.6:c.976-267_976-265dup ENSP00000222271.2:n.976-267_976-265dup
ENST00000425807.1:c.817-267_817-265dup ENSP00000403792.1:n.817-267_817-265dup
ENST00000542601.6:c.877-267_877-265dup ENSP00000439156.2:n.877-267_877-265dup
NM_000095.2:c.976-267_976-265dup NP_000086.2:n.976-267_976-265dup
NM_000095.3:c.976-267_976-265dup MANE Select NP_000086.2:n.976-267_976-265dup
Search 100 bp 5'
Search 100 bp 3'