Canonical Allele Identifier: CA2326526427

Gene: COMP

Linked Data

• dbSNP Id: rs2055178998

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787855_18787856insCT , CM000681.2:g.18787855_18787856insCT	GRCh38
NC_000019.9:g.18898664_18898665insCT , CM000681.1:g.18898664_18898665insCT	GRCh37
NC_000019.8:g.18759664_18759665insCT	NCBI36
NG_007070.1:g.8451_8452insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-205_976-204insGA MANE Select	ENSP00000222271.2:n.976-205_976-204insGA
ENST00000222271.6:c.976-205_976-204insGA	ENSP00000222271.2:n.976-205_976-204insGA
ENST00000425807.1:c.817-205_817-204insGA	ENSP00000403792.1:n.817-205_817-204insGA
ENST00000542601.6:c.877-205_877-204insGA	ENSP00000439156.2:n.877-205_877-204insGA
NM_000095.2:c.976-205_976-204insGA	NP_000086.2:n.976-205_976-204insGA
NM_000095.3:c.976-205_976-204insGA MANE Select	NP_000086.2:n.976-205_976-204insGA