Canonical Allele Identifier: CA2326526556

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787900_18787906delinsTTCTTTC , CM000681.2:g.18787900_18787906delinsTTCTTTC	GRCh38
NC_000019.9:g.18898709_18898715delinsTTCTTTC , CM000681.1:g.18898709_18898715delinsTTCTTTC	GRCh37
NC_000019.8:g.18759709_18759715delinsTTCTTTC	NCBI36
NG_007070.1:g.8400_8406delinsGAAAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-256_976-250delinsGAAAGAA MANE Select	ENSP00000222271.2:n.976-256_976-250delinsGAAAGAA
ENST00000222271.6:c.976-256_976-250delinsGAAAGAA	ENSP00000222271.2:n.976-256_976-250delinsGAAAGAA
ENST00000425807.1:c.817-256_817-250delinsGAAAGAA	ENSP00000403792.1:n.817-256_817-250delinsGAAAGAA
ENST00000542601.6:c.877-256_877-250delinsGAAAGAA	ENSP00000439156.2:n.877-256_877-250delinsGAAAGAA
NM_000095.2:c.976-256_976-250delinsGAAAGAA	NP_000086.2:n.976-256_976-250delinsGAAAGAA
NM_000095.3:c.976-256_976-250delinsGAAAGAA MANE Select	NP_000086.2:n.976-256_976-250delinsGAAAGAA