Canonical Allele Identifier: CA2326526443

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787860_18787864delinsTTTTC , CM000681.2:g.18787860_18787864delinsTTTTC	GRCh38
NC_000019.9:g.18898669_18898673delinsTTTTC , CM000681.1:g.18898669_18898673delinsTTTTC	GRCh37
NC_000019.8:g.18759669_18759673delinsTTTTC	NCBI36
NG_007070.1:g.8442_8446delinsGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-214_976-210delinsGAAAA MANE Select	ENSP00000222271.2:n.976-214_976-210delinsGAAAA
ENST00000222271.6:c.976-214_976-210delinsGAAAA	ENSP00000222271.2:n.976-214_976-210delinsGAAAA
ENST00000425807.1:c.817-214_817-210delinsGAAAA	ENSP00000403792.1:n.817-214_817-210delinsGAAAA
ENST00000542601.6:c.877-214_877-210delinsGAAAA	ENSP00000439156.2:n.877-214_877-210delinsGAAAA
NM_000095.2:c.976-214_976-210delinsGAAAA	NP_000086.2:n.976-214_976-210delinsGAAAA
NM_000095.3:c.976-214_976-210delinsGAAAA MANE Select	NP_000086.2:n.976-214_976-210delinsGAAAA