Canonical Allele Identifier: CA2326526341

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787814_18787815delinsTC , CM000681.2:g.18787814_18787815delinsTC	GRCh38
NC_000019.9:g.18898623_18898624delinsTC , CM000681.1:g.18898623_18898624delinsTC	GRCh37
NC_000019.8:g.18759623_18759624delinsTC	NCBI36
NG_007070.1:g.8491_8492delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-165_976-164delinsGA MANE Select	ENSP00000222271.2:n.976-165_976-164delinsGA
ENST00000222271.6:c.976-165_976-164delinsGA	ENSP00000222271.2:n.976-165_976-164delinsGA
ENST00000425807.1:c.817-165_817-164delinsGA	ENSP00000403792.1:n.817-165_817-164delinsGA
ENST00000542601.6:c.877-165_877-164delinsGA	ENSP00000439156.2:n.877-165_877-164delinsGA
NM_000095.2:c.976-165_976-164delinsGA	NP_000086.2:n.976-165_976-164delinsGA
NM_000095.3:c.976-165_976-164delinsGA MANE Select	NP_000086.2:n.976-165_976-164delinsGA