Canonical Allele Identifier: CA2326526409

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787850_18787852delinsTTC , CM000681.2:g.18787850_18787852delinsTTC	GRCh38
NC_000019.9:g.18898659_18898661delinsTTC , CM000681.1:g.18898659_18898661delinsTTC	GRCh37
NC_000019.8:g.18759659_18759661delinsTTC	NCBI36
NG_007070.1:g.8454_8456delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-202_976-200delinsGAA MANE Select	ENSP00000222271.2:n.976-202_976-200delinsGAA
ENST00000222271.6:c.976-202_976-200delinsGAA	ENSP00000222271.2:n.976-202_976-200delinsGAA
ENST00000425807.1:c.817-202_817-200delinsGAA	ENSP00000403792.1:n.817-202_817-200delinsGAA
ENST00000542601.6:c.877-202_877-200delinsGAA	ENSP00000439156.2:n.877-202_877-200delinsGAA
NM_000095.2:c.976-202_976-200delinsGAA	NP_000086.2:n.976-202_976-200delinsGAA
NM_000095.3:c.976-202_976-200delinsGAA MANE Select	NP_000086.2:n.976-202_976-200delinsGAA