Canonical Allele Identifier: CA2326524972

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785132_18785133delinsGC , CM000681.2:g.18785132_18785133delinsGC	GRCh38
NC_000019.9:g.18895942_18895943delinsGC , CM000681.1:g.18895942_18895943delinsGC	GRCh37
NC_000019.8:g.18756942_18756943delinsGC	NCBI36
NG_007070.1:g.11172_11173delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1718-41_1718-40delinsGC MANE Select	ENSP00000222271.2:n.1718-41_1718-40delinsGC
ENST00000222271.6:c.1718-41_1718-40delinsGC	ENSP00000222271.2:n.1718-41_1718-40delinsGC
ENST00000425807.1:c.1559-41_1559-40delinsGC	ENSP00000403792.1:n.1559-41_1559-40delinsGC
ENST00000542601.6:c.1619-41_1619-40delinsGC	ENSP00000439156.2:n.1619-41_1619-40delinsGC
NM_000095.2:c.1718-41_1718-40delinsGC	NP_000086.2:n.1718-41_1718-40delinsGC
NM_000095.3:c.1718-41_1718-40delinsGC MANE Select	NP_000086.2:n.1718-41_1718-40delinsGC