Canonical Allele Identifier: CA2326526567

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787906_18787909delinsCTTT , CM000681.2:g.18787906_18787909delinsCTTT	GRCh38
NC_000019.9:g.18898715_18898718delinsCTTT , CM000681.1:g.18898715_18898718delinsCTTT	GRCh37
NC_000019.8:g.18759715_18759718delinsCTTT	NCBI36
NG_007070.1:g.8397_8400delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-259_976-256delinsAAAG MANE Select	ENSP00000222271.2:n.976-259_976-256delinsAAAG
ENST00000222271.6:c.976-259_976-256delinsAAAG	ENSP00000222271.2:n.976-259_976-256delinsAAAG
ENST00000425807.1:c.817-259_817-256delinsAAAG	ENSP00000403792.1:n.817-259_817-256delinsAAAG
ENST00000542601.6:c.877-259_877-256delinsAAAG	ENSP00000439156.2:n.877-259_877-256delinsAAAG
NM_000095.2:c.976-259_976-256delinsAAAG	NP_000086.2:n.976-259_976-256delinsAAAG
NM_000095.3:c.976-259_976-256delinsAAAG MANE Select	NP_000086.2:n.976-259_976-256delinsAAAG