Canonical Allele Identifier: CA2326526347

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787403_18787404delinsCA , CM000681.2:g.18787403_18787404delinsCA	GRCh38
NC_000019.9:g.18898212_18898213delinsCA , CM000681.1:g.18898212_18898213delinsCA	GRCh37
NC_000019.8:g.18759212_18759213delinsCA	NCBI36
NG_007070.1:g.8902_8903delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1135+87_1135+88delinsTG MANE Select	ENSP00000222271.2:n.1135+87_1135+88delinsTG
ENST00000222271.6:c.1135+87_1135+88delinsTG	ENSP00000222271.2:n.1135+87_1135+88delinsTG
ENST00000425807.1:c.976+87_976+88delinsTG	ENSP00000403792.1:n.976+87_976+88delinsTG
ENST00000542601.6:c.1036+87_1036+88delinsTG	ENSP00000439156.2:n.1036+87_1036+88delinsTG
NM_000095.2:c.1135+87_1135+88delinsTG	NP_000086.2:n.1135+87_1135+88delinsTG
NM_000095.3:c.1135+87_1135+88delinsTG MANE Select	NP_000086.2:n.1135+87_1135+88delinsTG