Canonical Allele Identifier: CA994238101

Gene: COMP

Linked Data

• dbSNP Id: rs2055181573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787918_18787919insGAGACAGAG , CM000681.2:g.18787918_18787919insGAGACAGAG	GRCh38
NC_000019.9:g.18898727_18898728insGAGACAGAG , CM000681.1:g.18898727_18898728insGAGACAGAG	GRCh37
NC_000019.8:g.18759727_18759728insGAGACAGAG	NCBI36
NG_007070.1:g.8387_8388insCTCTGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-269_976-268insCTCTGTCTC MANE Select	ENSP00000222271.2:n.976-269_976-268insCTCTGTCTC
ENST00000222271.6:c.976-269_976-268insCTCTGTCTC	ENSP00000222271.2:n.976-269_976-268insCTCTGTCTC
ENST00000425807.1:c.817-269_817-268insCTCTGTCTC	ENSP00000403792.1:n.817-269_817-268insCTCTGTCTC
ENST00000542601.6:c.877-269_877-268insCTCTGTCTC	ENSP00000439156.2:n.877-269_877-268insCTCTGTCTC
NM_000095.2:c.976-269_976-268insCTCTGTCTC	NP_000086.2:n.976-269_976-268insCTCTGTCTC
NM_000095.3:c.976-269_976-268insCTCTGTCTC MANE Select	NP_000086.2:n.976-269_976-268insCTCTGTCTC