Canonical Allele Identifier: CA2326526494

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787870_18787876delinsCTTTCTT , CM000681.2:g.18787870_18787876delinsCTTTCTT	GRCh38
NC_000019.9:g.18898679_18898685delinsCTTTCTT , CM000681.1:g.18898679_18898685delinsCTTTCTT	GRCh37
NC_000019.8:g.18759679_18759685delinsCTTTCTT	NCBI36
NG_007070.1:g.8430_8436delinsAAGAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-226_976-220delinsAAGAAAG MANE Select	ENSP00000222271.2:n.976-226_976-220delinsAAGAAAG
ENST00000222271.6:c.976-226_976-220delinsAAGAAAG	ENSP00000222271.2:n.976-226_976-220delinsAAGAAAG
ENST00000425807.1:c.817-226_817-220delinsAAGAAAG	ENSP00000403792.1:n.817-226_817-220delinsAAGAAAG
ENST00000542601.6:c.877-226_877-220delinsAAGAAAG	ENSP00000439156.2:n.877-226_877-220delinsAAGAAAG
NM_000095.2:c.976-226_976-220delinsAAGAAAG	NP_000086.2:n.976-226_976-220delinsAAGAAAG
NM_000095.3:c.976-226_976-220delinsAAGAAAG MANE Select	NP_000086.2:n.976-226_976-220delinsAAGAAAG