Canonical Allele Identifier: CA2326526448

Gene: COMP

Linked Data

• dbSNP Id: rs2055179093

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787861_18787862insCT , CM000681.2:g.18787861_18787862insCT	GRCh38
NC_000019.9:g.18898670_18898671insCT , CM000681.1:g.18898670_18898671insCT	GRCh37
NC_000019.8:g.18759670_18759671insCT	NCBI36
NG_007070.1:g.8445_8446insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-211_976-210insGA MANE Select	ENSP00000222271.2:n.976-211_976-210insGA
ENST00000222271.6:c.976-211_976-210insGA	ENSP00000222271.2:n.976-211_976-210insGA
ENST00000425807.1:c.817-211_817-210insGA	ENSP00000403792.1:n.817-211_817-210insGA
ENST00000542601.6:c.877-211_877-210insGA	ENSP00000439156.2:n.877-211_877-210insGA
NM_000095.2:c.976-211_976-210insGA	NP_000086.2:n.976-211_976-210insGA
NM_000095.3:c.976-211_976-210insGA MANE Select	NP_000086.2:n.976-211_976-210insGA