Canonical Allele Identifier: CA2326525586

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786151_18786154delinsAGTG , CM000681.2:g.18786151_18786154delinsAGTG	GRCh38
NC_000019.9:g.18896961_18896964delinsAGTG , CM000681.1:g.18896961_18896964delinsAGTG	GRCh37
NC_000019.8:g.18757961_18757964delinsAGTG	NCBI36
NG_007070.1:g.10151_10154delinsCACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.1308-8_1308-5delinsCACT MANE Select	ENSP00000222271.2:n.1308-8_1308-5delinsCACT
ENST00000222271.6:c.1308-8_1308-5delinsCACT	ENSP00000222271.2:n.1308-8_1308-5delinsCACT
ENST00000425807.1:c.1149-8_1149-5delinsCACT	ENSP00000403792.1:n.1149-8_1149-5delinsCACT
ENST00000542601.6:c.1209-8_1209-5delinsCACT	ENSP00000439156.2:n.1209-8_1209-5delinsCACT
ENST00000612179.1:n.558-8_558-5delinsCACT
NM_000095.2:c.1308-8_1308-5delinsCACT	NP_000086.2:n.1308-8_1308-5delinsCACT
NM_000095.3:c.1308-8_1308-5delinsCACT MANE Select	NP_000086.2:n.1308-8_1308-5delinsCACT