Canonical Allele Identifier: CA783973384
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1555791614
MyVariant Identifiers: chr19:g.18898680_18898681insTC (hg19) chr19:g.18787871_18787872insTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787872_18787873insCT , CM000681.2:g.18787872_18787873insCT GRCh38
NC_000019.9:g.18898681_18898682insCT , CM000681.1:g.18898681_18898682insCT GRCh37
NC_000019.8:g.18759681_18759682insCT NCBI36
NG_007070.1:g.8434_8435insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-222_976-221insGA MANE Select ENSP00000222271.2:n.976-222_976-221insGA
ENST00000222271.6:c.976-222_976-221insGA ENSP00000222271.2:n.976-222_976-221insGA
ENST00000425807.1:c.817-222_817-221insGA ENSP00000403792.1:n.817-222_817-221insGA
ENST00000542601.6:c.877-222_877-221insGA ENSP00000439156.2:n.877-222_877-221insGA
NM_000095.2:c.976-222_976-221insGA NP_000086.2:n.976-222_976-221insGA
NM_000095.3:c.976-222_976-221insGA MANE Select NP_000086.2:n.976-222_976-221insGA
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