Canonical Allele Identifier: CA2735646787

Gene: COMP

Linked Data

• dbSNP Id: rs1365200158

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787849_18787851del , CM000681.2:g.18787849_18787851del	GRCh38
NC_000019.9:g.18898658_18898660del , CM000681.1:g.18898658_18898660del	GRCh37
NC_000019.8:g.18759658_18759660del	NCBI36
NG_007070.1:g.8458_8460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-198_976-196del MANE Select	ENSP00000222271.2:n.976-198_976-196del
ENST00000222271.6:c.976-198_976-196del	ENSP00000222271.2:n.976-198_976-196del
ENST00000425807.1:c.817-198_817-196del	ENSP00000403792.1:n.817-198_817-196del
ENST00000542601.6:c.877-198_877-196del	ENSP00000439156.2:n.877-198_877-196del
NM_000095.2:c.976-198_976-196del	NP_000086.2:n.976-198_976-196del
NM_000095.3:c.976-198_976-196del MANE Select	NP_000086.2:n.976-198_976-196del