Canonical Allele Identifier: CA994237997

Gene: COMP

Linked Data

• gnomAD v3: 19-18787906-C-CTTTTTTTT
• gnomAD v4: 19-18787906-C-CTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787909_18787910insTTTTTTTT , CM000681.2:g.18787909_18787910insTTTTTTTT	GRCh38
NC_000019.9:g.18898718_18898719insTTTTTTTT , CM000681.1:g.18898718_18898719insTTTTTTTT	GRCh37
NC_000019.8:g.18759718_18759719insTTTTTTTT	NCBI36
NG_007070.1:g.8399_8400insAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-257_976-256insAAAAAAAA MANE Select	ENSP00000222271.2:n.976-257_976-256insAAAAAAAA
ENST00000222271.6:c.976-257_976-256insAAAAAAAA	ENSP00000222271.2:n.976-257_976-256insAAAAAAAA
ENST00000425807.1:c.817-257_817-256insAAAAAAAA	ENSP00000403792.1:n.817-257_817-256insAAAAAAAA
ENST00000542601.6:c.877-257_877-256insAAAAAAAA	ENSP00000439156.2:n.877-257_877-256insAAAAAAAA
NM_000095.2:c.976-257_976-256insAAAAAAAA	NP_000086.2:n.976-257_976-256insAAAAAAAA
NM_000095.3:c.976-257_976-256insAAAAAAAA MANE Select	NP_000086.2:n.976-257_976-256insAAAAAAAA