Canonical Allele Identifier: CA2576725772

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785925_18785929del , CM000681.2:g.18785925_18785929del	GRCh38
NC_000019.9:g.18896735_18896739del , CM000681.1:g.18896735_18896739del	GRCh37
NC_000019.8:g.18757735_18757739del	NCBI36
NG_007070.1:g.10376_10380del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1489+36_1489+40del MANE Select	ENSP00000222271.2:n.1489+36_1489+40del
ENST00000222271.6:c.1489+36_1489+40del	ENSP00000222271.2:n.1489+36_1489+40del
ENST00000425807.1:c.1330+36_1330+40del	ENSP00000403792.1:n.1330+36_1330+40del
ENST00000542601.6:c.1390+36_1390+40del	ENSP00000439156.2:n.1390+36_1390+40del
NM_000095.2:c.1489+36_1489+40del	NP_000086.2:n.1489+36_1489+40del
NM_000095.3:c.1489+36_1489+40del MANE Select	NP_000086.2:n.1489+36_1489+40del