Canonical Allele Identifier: CA2326527283

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789288G= , CM000681.2:g.18789288G=	GRCh38
NC_000019.9:g.18900097G= , CM000681.1:g.18900097G=	GRCh37
NC_000019.8:g.18761097G=	NCBI36
NG_007070.1:g.7018C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.400C= MANE Select	ENSP00000222271.2:p.His134=
ENST00000222271.6:c.400C=	ENSP00000222271.2:p.His134=
ENST00000425807.1:c.391-396C=	ENSP00000403792.1:n.391-396C=
ENST00000542601.6:c.301C=	ENSP00000439156.2:p.His101=
NM_000095.2:c.400C=	NP_000086.2:p.His134=
NM_000095.3:c.400C= MANE Select	NP_000086.2:p.His134=