Canonical Allele Identifier: CA2326526440

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787860_18787870delinsTTTTCTCTTTC , CM000681.2:g.18787860_18787870delinsTTTTCTCTTTC	GRCh38
NC_000019.9:g.18898669_18898679delinsTTTTCTCTTTC , CM000681.1:g.18898669_18898679delinsTTTTCTCTTTC	GRCh37
NC_000019.8:g.18759669_18759679delinsTTTTCTCTTTC	NCBI36
NG_007070.1:g.8436_8446delinsGAAAGAGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-220_976-210delinsGAAAGAGAAAA MANE Select	ENSP00000222271.2:n.976-220_976-210delinsGAAAGAGAAAA
ENST00000222271.6:c.976-220_976-210delinsGAAAGAGAAAA	ENSP00000222271.2:n.976-220_976-210delinsGAAAGAGAAAA
ENST00000425807.1:c.817-220_817-210delinsGAAAGAGAAAA	ENSP00000403792.1:n.817-220_817-210delinsGAAAGAGAAAA
ENST00000542601.6:c.877-220_877-210delinsGAAAGAGAAAA	ENSP00000439156.2:n.877-220_877-210delinsGAAAGAGAAAA
NM_000095.2:c.976-220_976-210delinsGAAAGAGAAAA	NP_000086.2:n.976-220_976-210delinsGAAAGAGAAAA
NM_000095.3:c.976-220_976-210delinsGAAAGAGAAAA MANE Select	NP_000086.2:n.976-220_976-210delinsGAAAGAGAAAA