Canonical Allele Identifier: CA2326524842

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18784845T= , CM000681.2:g.18784845T=	GRCh38
NC_000019.9:g.18895655T= , CM000681.1:g.18895655T=	GRCh37
NC_000019.8:g.18756655T=	NCBI36
NG_007070.1:g.11460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1914+51A= MANE Select	ENSP00000222271.2:n.1914+51A=
ENST00000222271.6:c.1914+51A=	ENSP00000222271.2:n.1914+51A=
ENST00000425807.1:c.1755+51A=	ENSP00000403792.1:n.1755+51A=
ENST00000542601.6:c.1815+51A=	ENSP00000439156.2:n.1815+51A=
NM_000095.2:c.1914+51A=	NP_000086.2:n.1914+51A=
NM_000095.3:c.1914+51A= MANE Select	NP_000086.2:n.1914+51A=