Canonical Allele Identifier: CA2326526382

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787445_18787446delinsCG , CM000681.2:g.18787445_18787446delinsCG	GRCh38
NC_000019.9:g.18898254_18898255delinsCG , CM000681.1:g.18898254_18898255delinsCG	GRCh37
NC_000019.8:g.18759254_18759255delinsCG	NCBI36
NG_007070.1:g.8860_8861delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1135+45_1135+46delinsCG MANE Select	ENSP00000222271.2:n.1135+45_1135+46delinsCG
ENST00000222271.6:c.1135+45_1135+46delinsCG	ENSP00000222271.2:n.1135+45_1135+46delinsCG
ENST00000425807.1:c.976+45_976+46delinsCG	ENSP00000403792.1:n.976+45_976+46delinsCG
ENST00000542601.6:c.1036+45_1036+46delinsCG	ENSP00000439156.2:n.1036+45_1036+46delinsCG
NM_000095.2:c.1135+45_1135+46delinsCG	NP_000086.2:n.1135+45_1135+46delinsCG
NM_000095.3:c.1135+45_1135+46delinsCG MANE Select	NP_000086.2:n.1135+45_1135+46delinsCG