Canonical Allele Identifier: CA2326525583

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786150_18786157delinsGAGTGGAT , CM000681.2:g.18786150_18786157delinsGAGTGGAT	GRCh38
NC_000019.9:g.18896960_18896967delinsGAGTGGAT , CM000681.1:g.18896960_18896967delinsGAGTGGAT	GRCh37
NC_000019.8:g.18757960_18757967delinsGAGTGGAT	NCBI36
NG_007070.1:g.10148_10155delinsATCCACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1308-11_1308-4delinsATCCACTC MANE Select	ENSP00000222271.2:n.1308-11_1308-4delinsATCCACTC
ENST00000222271.6:c.1308-11_1308-4delinsATCCACTC	ENSP00000222271.2:n.1308-11_1308-4delinsATCCACTC
ENST00000425807.1:c.1149-11_1149-4delinsATCCACTC	ENSP00000403792.1:n.1149-11_1149-4delinsATCCACTC
ENST00000542601.6:c.1209-11_1209-4delinsATCCACTC	ENSP00000439156.2:n.1209-11_1209-4delinsATCCACTC
ENST00000612179.1:n.558-11_558-4delinsATCCACTC
NM_000095.2:c.1308-11_1308-4delinsATCCACTC	NP_000086.2:n.1308-11_1308-4delinsATCCACTC
NM_000095.3:c.1308-11_1308-4delinsATCCACTC MANE Select	NP_000086.2:n.1308-11_1308-4delinsATCCACTC