Canonical Allele Identifier: CA2326526399

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787845_18787846delinsCT , CM000681.2:g.18787845_18787846delinsCT	GRCh38
NC_000019.9:g.18898654_18898655delinsCT , CM000681.1:g.18898654_18898655delinsCT	GRCh37
NC_000019.8:g.18759654_18759655delinsCT	NCBI36
NG_007070.1:g.8460_8461delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-196_976-195delinsAG MANE Select	ENSP00000222271.2:n.976-196_976-195delinsAG
ENST00000222271.6:c.976-196_976-195delinsAG	ENSP00000222271.2:n.976-196_976-195delinsAG
ENST00000425807.1:c.817-196_817-195delinsAG	ENSP00000403792.1:n.817-196_817-195delinsAG
ENST00000542601.6:c.877-196_877-195delinsAG	ENSP00000439156.2:n.877-196_877-195delinsAG
NM_000095.2:c.976-196_976-195delinsAG	NP_000086.2:n.976-196_976-195delinsAG
NM_000095.3:c.976-196_976-195delinsAG MANE Select	NP_000086.2:n.976-196_976-195delinsAG