Canonical Allele Identifier: CA2326525571

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786123G= , CM000681.2:g.18786123G=	GRCh38
NC_000019.9:g.18896933G= , CM000681.1:g.18896933G=	GRCh37
NC_000019.8:g.18757933G=	NCBI36
NG_007070.1:g.10182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1331C= MANE Select	ENSP00000222271.2:p.Ser444=
ENST00000222271.6:c.1331C=	ENSP00000222271.2:p.Ser444=
ENST00000425807.1:c.1172C=	ENSP00000403792.1:p.Ser391=
ENST00000542601.6:c.1232C=	ENSP00000439156.2:p.Ser411=
ENST00000612179.1:n.581C=
NM_000095.2:c.1331C=	NP_000086.2:p.Ser444=
NM_000095.3:c.1331C= MANE Select	NP_000086.2:p.Ser444=