Canonical Allele Identifier: CA2326526213

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787681_18787690delinsCAGGTCGAGA , CM000681.2:g.18787681_18787690delinsCAGGTCGAGA	GRCh38
NC_000019.9:g.18898490_18898499delinsCAGGTCGAGA , CM000681.1:g.18898490_18898499delinsCAGGTCGAGA	GRCh37
NC_000019.8:g.18759490_18759499delinsCAGGTCGAGA	NCBI36
NG_007070.1:g.8616_8625delinsTCTCGACCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-40_976-31delinsTCTCGACCTG MANE Select	ENSP00000222271.2:n.976-40_976-31delinsTCTCGACCTG
ENST00000222271.6:c.976-40_976-31delinsTCTCGACCTG	ENSP00000222271.2:n.976-40_976-31delinsTCTCGACCTG
ENST00000425807.1:c.817-40_817-31delinsTCTCGACCTG	ENSP00000403792.1:n.817-40_817-31delinsTCTCGACCTG
ENST00000542601.6:c.877-40_877-31delinsTCTCGACCTG	ENSP00000439156.2:n.877-40_877-31delinsTCTCGACCTG
NM_000095.2:c.976-40_976-31delinsTCTCGACCTG	NP_000086.2:n.976-40_976-31delinsTCTCGACCTG
NM_000095.3:c.976-40_976-31delinsTCTCGACCTG MANE Select	NP_000086.2:n.976-40_976-31delinsTCTCGACCTG