Canonical Allele Identifier: CA2326527262

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789235G= , CM000681.2:g.18789235G=	GRCh38
NC_000019.9:g.18900044G= , CM000681.1:g.18900044G=	GRCh37
NC_000019.8:g.18761044G=	NCBI36
NG_007070.1:g.7071C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.453C= MANE Select	ENSP00000222271.2:p.Cys151=
ENST00000222271.6:c.453C=	ENSP00000222271.2:p.Cys151=
ENST00000425807.1:c.391-343C=	ENSP00000403792.1:n.391-343C=
ENST00000542601.6:c.354C=	ENSP00000439156.2:p.Cys118=
NM_000095.2:c.453C=	NP_000086.2:p.Cys151=
NM_000095.3:c.453C= MANE Select	NP_000086.2:p.Cys151=