Canonical Allele Identifier: CA2326524854

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18784870_18784871delinsAG , CM000681.2:g.18784870_18784871delinsAG	GRCh38
NC_000019.9:g.18895680_18895681delinsAG , CM000681.1:g.18895680_18895681delinsAG	GRCh37
NC_000019.8:g.18756680_18756681delinsAG	NCBI36
NG_007070.1:g.11434_11435delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1914+25_1914+26delinsCT MANE Select	ENSP00000222271.2:n.1914+25_1914+26delinsCT
ENST00000222271.6:c.1914+25_1914+26delinsCT	ENSP00000222271.2:n.1914+25_1914+26delinsCT
ENST00000425807.1:c.1755+25_1755+26delinsCT	ENSP00000403792.1:n.1755+25_1755+26delinsCT
ENST00000542601.6:c.1815+25_1815+26delinsCT	ENSP00000439156.2:n.1815+25_1815+26delinsCT
NM_000095.2:c.1914+25_1914+26delinsCT	NP_000086.2:n.1914+25_1914+26delinsCT
NM_000095.3:c.1914+25_1914+26delinsCT MANE Select	NP_000086.2:n.1914+25_1914+26delinsCT