Canonical Allele Identifier: CA783973306
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1555791599
MyVariant Identifiers: chr19:g.18898649_18898650insTTTTCTT (hg19) chr19:g.18787840_18787841insTTTTCTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787851_18787857dup , CM000681.2:g.18787851_18787857dup GRCh38
NC_000019.9:g.18898660_18898666dup , CM000681.1:g.18898660_18898666dup GRCh37
NC_000019.8:g.18759660_18759666dup NCBI36
NG_007070.1:g.8459_8465dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-197_976-191dup MANE Select ENSP00000222271.2:n.976-197_976-191dup
ENST00000222271.6:c.976-197_976-191dup ENSP00000222271.2:n.976-197_976-191dup
ENST00000425807.1:c.817-197_817-191dup ENSP00000403792.1:n.817-197_817-191dup
ENST00000542601.6:c.877-197_877-191dup ENSP00000439156.2:n.877-197_877-191dup
NM_000095.2:c.976-197_976-191dup NP_000086.2:n.976-197_976-191dup
NM_000095.3:c.976-197_976-191dup MANE Select NP_000086.2:n.976-197_976-191dup
Search 100 bp 5'
Search 100 bp 3'