Canonical Allele Identifier: CA2326524832

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18784825_18784826delinsGT , CM000681.2:g.18784825_18784826delinsGT	GRCh38
NC_000019.9:g.18895635_18895636delinsGT , CM000681.1:g.18895635_18895636delinsGT	GRCh37
NC_000019.8:g.18756635_18756636delinsGT	NCBI36
NG_007070.1:g.11479_11480delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1914+70_1914+71delinsAC MANE Select	ENSP00000222271.2:n.1914+70_1914+71delinsAC
ENST00000222271.6:c.1914+70_1914+71delinsAC	ENSP00000222271.2:n.1914+70_1914+71delinsAC
ENST00000425807.1:c.1755+70_1755+71delinsAC	ENSP00000403792.1:n.1755+70_1755+71delinsAC
ENST00000542601.6:c.1815+70_1815+71delinsAC	ENSP00000439156.2:n.1815+70_1815+71delinsAC
NM_000095.2:c.1914+70_1914+71delinsAC	NP_000086.2:n.1914+70_1914+71delinsAC
NM_000095.3:c.1914+70_1914+71delinsAC MANE Select	NP_000086.2:n.1914+70_1914+71delinsAC