Canonical Allele Identifier: CA2326526563

Gene: COMP

Linked Data

• dbSNP Id: rs2055181123

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787906_18787908del , CM000681.2:g.18787906_18787908del	GRCh38
NC_000019.9:g.18898715_18898717del , CM000681.1:g.18898715_18898717del	GRCh37
NC_000019.8:g.18759715_18759717del	NCBI36
NG_007070.1:g.8400_8402del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-256_976-254del MANE Select	ENSP00000222271.2:n.976-256_976-254del
ENST00000222271.6:c.976-256_976-254del	ENSP00000222271.2:n.976-256_976-254del
ENST00000425807.1:c.817-256_817-254del	ENSP00000403792.1:n.817-256_817-254del
ENST00000542601.6:c.877-256_877-254del	ENSP00000439156.2:n.877-256_877-254del
NM_000095.2:c.976-256_976-254del	NP_000086.2:n.976-256_976-254del
NM_000095.3:c.976-256_976-254del MANE Select	NP_000086.2:n.976-256_976-254del