Canonical Allele Identifier: CA2326526442

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787860_18787866delinsTTTTCTC , CM000681.2:g.18787860_18787866delinsTTTTCTC	GRCh38
NC_000019.9:g.18898669_18898675delinsTTTTCTC , CM000681.1:g.18898669_18898675delinsTTTTCTC	GRCh37
NC_000019.8:g.18759669_18759675delinsTTTTCTC	NCBI36
NG_007070.1:g.8440_8446delinsGAGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-216_976-210delinsGAGAAAA MANE Select	ENSP00000222271.2:n.976-216_976-210delinsGAGAAAA
ENST00000222271.6:c.976-216_976-210delinsGAGAAAA	ENSP00000222271.2:n.976-216_976-210delinsGAGAAAA
ENST00000425807.1:c.817-216_817-210delinsGAGAAAA	ENSP00000403792.1:n.817-216_817-210delinsGAGAAAA
ENST00000542601.6:c.877-216_877-210delinsGAGAAAA	ENSP00000439156.2:n.877-216_877-210delinsGAGAAAA
NM_000095.2:c.976-216_976-210delinsGAGAAAA	NP_000086.2:n.976-216_976-210delinsGAGAAAA
NM_000095.3:c.976-216_976-210delinsGAGAAAA MANE Select	NP_000086.2:n.976-216_976-210delinsGAGAAAA