Canonical Allele Identifier: CA2326525468

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785934_18785935delinsGC , CM000681.2:g.18785934_18785935delinsGC	GRCh38
NC_000019.9:g.18896744_18896745delinsGC , CM000681.1:g.18896744_18896745delinsGC	GRCh37
NC_000019.8:g.18757744_18757745delinsGC	NCBI36
NG_007070.1:g.10370_10371delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1489+30_1489+31delinsGC MANE Select	ENSP00000222271.2:n.1489+30_1489+31delinsGC
ENST00000222271.6:c.1489+30_1489+31delinsGC	ENSP00000222271.2:n.1489+30_1489+31delinsGC
ENST00000425807.1:c.1330+30_1330+31delinsGC	ENSP00000403792.1:n.1330+30_1330+31delinsGC
ENST00000542601.6:c.1390+30_1390+31delinsGC	ENSP00000439156.2:n.1390+30_1390+31delinsGC
NM_000095.2:c.1489+30_1489+31delinsGC	NP_000086.2:n.1489+30_1489+31delinsGC
NM_000095.3:c.1489+30_1489+31delinsGC MANE Select	NP_000086.2:n.1489+30_1489+31delinsGC