Canonical Allele Identifier: CA2741617857
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784941_18784942insCCC , CM000681.2:g.18784941_18784942insCCC GRCh38
NC_000019.9:g.18895751_18895752insCCC , CM000681.1:g.18895751_18895752insCCC GRCh37
NC_000019.8:g.18756751_18756752insCCC NCBI36
NG_007070.1:g.11365_11366insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1870_1871insGGG MANE Select ENSP00000222271.2:p.Gln623_Ala624insGly
ENST00000222271.6:c.1870_1871insGGG ENSP00000222271.2:p.Gln623_Ala624insGly
ENST00000425807.1:c.1711_1712insGGG ENSP00000403792.1:p.Gln570_Ala571insGly
ENST00000542601.6:c.1771_1772insGGG ENSP00000439156.2:p.Gln590_Ala591insGly
NM_000095.2:c.1870_1871insGGG NP_000086.2:p.Gln623_Ala624insGly
NM_000095.3:c.1870_1871insGGG MANE Select NP_000086.2:p.Gln623_Ala624insGly
Search 100 bp 5'
Search 100 bp 3'