Canonical Allele Identifier: CA2326525366

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785762T= , CM000681.2:g.18785762T=	GRCh38
NC_000019.9:g.18896572T= , CM000681.1:g.18896572T=	GRCh37
NC_000019.8:g.18757572T=	NCBI36
NG_007070.1:g.10543A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1579A= MANE Select	ENSP00000222271.2:p.Thr527=
ENST00000222271.6:c.1579A=	ENSP00000222271.2:p.Thr527=
ENST00000425807.1:c.1420A=	ENSP00000403792.1:p.Thr474=
ENST00000542601.6:c.1480A=	ENSP00000439156.2:p.Thr494=
NM_000095.2:c.1579A=	NP_000086.2:p.Thr527=
NM_000095.3:c.1579A= MANE Select	NP_000086.2:p.Thr527=