Canonical Allele Identifier: CA2326527253

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789223C= , CM000681.2:g.18789223C=	GRCh38
NC_000019.9:g.18900032C= , CM000681.1:g.18900032C=	GRCh37
NC_000019.8:g.18761032C=	NCBI36
NG_007070.1:g.7083G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.465G= MANE Select	ENSP00000222271.2:p.Pro155=
ENST00000222271.6:c.465G=	ENSP00000222271.2:p.Pro155=
ENST00000425807.1:c.391-331G=	ENSP00000403792.1:n.391-331G=
ENST00000542601.6:c.366G=	ENSP00000439156.2:p.Pro122=
NM_000095.2:c.465G=	NP_000086.2:p.Pro155=
NM_000095.3:c.465G= MANE Select	NP_000086.2:p.Pro155=