Canonical Allele Identifier: CA2582001308
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs2145902694
gnomAD v3: 19-18787871-TTTC-T
gnomAD v4: 19-18787871-TTTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787874_18787876del , CM000681.2:g.18787874_18787876del GRCh38
NC_000019.9:g.18898683_18898685del , CM000681.1:g.18898683_18898685del GRCh37
NC_000019.8:g.18759683_18759685del NCBI36
NG_007070.1:g.8432_8434del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-224_976-222del MANE Select ENSP00000222271.2:n.976-224_976-222del
ENST00000222271.6:c.976-224_976-222del ENSP00000222271.2:n.976-224_976-222del
ENST00000425807.1:c.817-224_817-222del ENSP00000403792.1:n.817-224_817-222del
ENST00000542601.6:c.877-224_877-222del ENSP00000439156.2:n.877-224_877-222del
NM_000095.2:c.976-224_976-222del NP_000086.2:n.976-224_976-222del
NM_000095.3:c.976-224_976-222del MANE Select NP_000086.2:n.976-224_976-222del
Search 100 bp 5'
Search 100 bp 3'