Canonical Allele Identifier: CA2326526514

Gene: COMP

Linked Data

• dbSNP Id: rs2055180320

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787876_18787881del , CM000681.2:g.18787876_18787881del	GRCh38
NC_000019.9:g.18898685_18898690del , CM000681.1:g.18898685_18898690del	GRCh37
NC_000019.8:g.18759685_18759690del	NCBI36
NG_007070.1:g.8426_8431del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-230_976-225del MANE Select	ENSP00000222271.2:n.976-230_976-225del
ENST00000222271.6:c.976-230_976-225del	ENSP00000222271.2:n.976-230_976-225del
ENST00000425807.1:c.817-230_817-225del	ENSP00000403792.1:n.817-230_817-225del
ENST00000542601.6:c.877-230_877-225del	ENSP00000439156.2:n.877-230_877-225del
NM_000095.2:c.976-230_976-225del	NP_000086.2:n.976-230_976-225del
NM_000095.3:c.976-230_976-225del MANE Select	NP_000086.2:n.976-230_976-225del