Canonical Allele Identifier: CA2583621639

Gene: COMP

Linked Data

• gnomAD v4: 19-18785197-G-GAGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785198_18785199insGGTA , CM000681.2:g.18785198_18785199insGGTA	GRCh38
NC_000019.9:g.18896008_18896009insGGTA , CM000681.1:g.18896008_18896009insGGTA	GRCh37
NC_000019.8:g.18757008_18757009insGGTA	NCBI36
NG_007070.1:g.11107_11108insACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1718-106_1718-105insACCT MANE Select	ENSP00000222271.2:n.1718-106_1718-105insACCT
ENST00000222271.6:c.1718-106_1718-105insACCT	ENSP00000222271.2:n.1718-106_1718-105insACCT
ENST00000425807.1:c.1559-106_1559-105insACCT	ENSP00000403792.1:n.1559-106_1559-105insACCT
ENST00000542601.6:c.1619-106_1619-105insACCT	ENSP00000439156.2:n.1619-106_1619-105insACCT
NM_000095.2:c.1718-106_1718-105insACCT	NP_000086.2:n.1718-106_1718-105insACCT
NM_000095.3:c.1718-106_1718-105insACCT MANE Select	NP_000086.2:n.1718-106_1718-105insACCT