Canonical Allele Identifier: CA2695228440
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787508_18787513del , CM000681.2:g.18787508_18787513del GRCh38
NC_000019.9:g.18898317_18898322del , CM000681.1:g.18898317_18898322del GRCh37
NC_000019.8:g.18759317_18759322del NCBI36
NG_007070.1:g.8797_8802del

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1117_1122del MANE Select ENSP00000222271.2:p.Asp373_Asp374del
ENST00000222271.6:c.1117_1122del ENSP00000222271.2:p.Asp373_Asp374del
ENST00000425807.1:c.958_963del ENSP00000403792.1:p.Asp320_Asp321del
ENST00000542601.6:c.1018_1023del ENSP00000439156.2:p.Asp340_Asp341del
NM_000095.2:c.1117_1122del NP_000086.2:p.Asp373_Asp374del
NM_000095.3:c.1117_1122del MANE Select NP_000086.2:p.Asp373_Asp374del