Canonical Allele Identifier: CA2326526086
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787599_18787605delinsTGTCCTC , CM000681.2:g.18787599_18787605delinsTGTCCTC GRCh38
NC_000019.9:g.18898408_18898414delinsTGTCCTC , CM000681.1:g.18898408_18898414delinsTGTCCTC GRCh37
NC_000019.8:g.18759408_18759414delinsTGTCCTC NCBI36
NG_007070.1:g.8701_8707delinsGAGGACA

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1021_1027delinsGAGGACA MANE Select ENSP00000222271.2:p.Glu341=
ENST00000222271.6:c.1021_1027delinsGAGGACA ENSP00000222271.2:p.Glu341=
ENST00000425807.1:c.862_868delinsGAGGACA ENSP00000403792.1:p.Glu288=
ENST00000542601.6:c.922_928delinsGAGGACA ENSP00000439156.2:p.Glu308=
NM_000095.2:c.1021_1027delinsGAGGACA NP_000086.2:p.Glu341=
NM_000095.3:c.1021_1027delinsGAGGACA MANE Select NP_000086.2:p.Glu341=