Canonical Allele Identifier: CA2326526203

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787676G= , CM000681.2:g.18787676G=	GRCh38
NC_000019.9:g.18898485G= , CM000681.1:g.18898485G=	GRCh37
NC_000019.8:g.18759485G=	NCBI36
NG_007070.1:g.8630C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-26C= MANE Select	ENSP00000222271.2:n.976-26C=
ENST00000222271.6:c.976-26C=	ENSP00000222271.2:n.976-26C=
ENST00000425807.1:c.817-26C=	ENSP00000403792.1:n.817-26C=
ENST00000542601.6:c.877-26C=	ENSP00000439156.2:n.877-26C=
NM_000095.2:c.976-26C=	NP_000086.2:n.976-26C=
NM_000095.3:c.976-26C= MANE Select	NP_000086.2:n.976-26C=