Canonical Allele Identifier: CA2580096748
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2089820
ClinVar RCV Id: RCV003020597

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787502_18787507del , CM000681.2:g.18787502_18787507del GRCh38
NC_000019.9:g.18898311_18898316del , CM000681.1:g.18898311_18898316del GRCh37
NC_000019.8:g.18759311_18759316del NCBI36
NG_007070.1:g.8803_8808del

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1123_1128del MANE Select ENSP00000222271.2:p.Ile375_Asp376del
ENST00000222271.6:c.1123_1128del ENSP00000222271.2:p.Ile375_Asp376del
ENST00000425807.1:c.964_969del ENSP00000403792.1:p.Ile322_Asp323del
ENST00000542601.6:c.1024_1029del ENSP00000439156.2:p.Ile342_Asp343del
NM_000095.2:c.1123_1128del NP_000086.2:p.Ile375_Asp376del
NM_000095.3:c.1123_1128del MANE Select NP_000086.2:p.Ile375_Asp376del