Canonical Allele Identifier: CA2326524951

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785095_18785096delinsAG , CM000681.2:g.18785095_18785096delinsAG	GRCh38
NC_000019.9:g.18895905_18895906delinsAG , CM000681.1:g.18895905_18895906delinsAG	GRCh37
NC_000019.8:g.18756905_18756906delinsAG	NCBI36
NG_007070.1:g.11209_11210delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1718-4_1718-3delinsCT MANE Select	ENSP00000222271.2:n.1718-4_1718-3delinsCT
ENST00000222271.6:c.1718-4_1718-3delinsCT	ENSP00000222271.2:n.1718-4_1718-3delinsCT
ENST00000425807.1:c.1559-4_1559-3delinsCT	ENSP00000403792.1:n.1559-4_1559-3delinsCT
ENST00000542601.6:c.1619-4_1619-3delinsCT	ENSP00000439156.2:n.1619-4_1619-3delinsCT
NM_000095.2:c.1718-4_1718-3delinsCT	NP_000086.2:n.1718-4_1718-3delinsCT
NM_000095.3:c.1718-4_1718-3delinsCT MANE Select	NP_000086.2:n.1718-4_1718-3delinsCT