Canonical Allele Identifier: CA632375838
Gene: COMP HGNC NCBI

Linked Data

gnomAD v2: 19-18898731-TGAGACAGAG-T
gnomAD v3: 19-18787922-TGAGACAGAG-T
gnomAD v4: 19-18787922-TGAGACAGAG-T
MyVariant Identifiers: chr19:g.18898732_18898740del (hg19) chr19:g.18787923_18787931del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787923_18787931del , CM000681.2:g.18787923_18787931del GRCh38
NC_000019.9:g.18898732_18898740del , CM000681.1:g.18898732_18898740del GRCh37
NC_000019.8:g.18759732_18759740del NCBI36
NG_007070.1:g.8375_8383del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-281_976-273del MANE Select ENSP00000222271.2:n.976-281_976-273del
ENST00000222271.6:c.976-281_976-273del ENSP00000222271.2:n.976-281_976-273del
ENST00000425807.1:c.817-281_817-273del ENSP00000403792.1:n.817-281_817-273del
ENST00000542601.6:c.877-281_877-273del ENSP00000439156.2:n.877-281_877-273del
NM_000095.2:c.976-281_976-273del NP_000086.2:n.976-281_976-273del
NM_000095.3:c.976-281_976-273del MANE Select NP_000086.2:n.976-281_976-273del
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