Canonical Allele Identifier: CA994238120
Gene: COMP HGNC NCBI

Linked Data

gnomAD v3: 19-18787920-TTTGAGACAGAG-T
gnomAD v4: 19-18787920-TTTGAGACAGAG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787922_18787932del , CM000681.2:g.18787922_18787932del GRCh38
NC_000019.9:g.18898731_18898741del , CM000681.1:g.18898731_18898741del GRCh37
NC_000019.8:g.18759731_18759741del NCBI36
NG_007070.1:g.8375_8385del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-281_976-271del MANE Select ENSP00000222271.2:n.976-281_976-271del
ENST00000222271.6:c.976-281_976-271del ENSP00000222271.2:n.976-281_976-271del
ENST00000425807.1:c.817-281_817-271del ENSP00000403792.1:n.817-281_817-271del
ENST00000542601.6:c.877-281_877-271del ENSP00000439156.2:n.877-281_877-271del
NM_000095.2:c.976-281_976-271del NP_000086.2:n.976-281_976-271del
NM_000095.3:c.976-281_976-271del MANE Select NP_000086.2:n.976-281_976-271del
Search 100 bp 5'
Search 100 bp 3'