Canonical Allele Identifier: CA2326527268

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789249G= , CM000681.2:g.18789249G=	GRCh38
NC_000019.9:g.18900058G= , CM000681.1:g.18900058G=	GRCh37
NC_000019.8:g.18761058G=	NCBI36
NG_007070.1:g.7057C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.439C= MANE Select	ENSP00000222271.2:p.Pro147=
ENST00000222271.6:c.439C=	ENSP00000222271.2:p.Pro147=
ENST00000425807.1:c.391-357C=	ENSP00000403792.1:n.391-357C=
ENST00000542601.6:c.340C=	ENSP00000439156.2:p.Pro114=
NM_000095.2:c.439C=	NP_000086.2:p.Pro147=
NM_000095.3:c.439C= MANE Select	NP_000086.2:p.Pro147=