Canonical Allele Identifier: CA2326524017

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18783135T= , CM000681.2:g.18783135T=	GRCh38
NC_000019.9:g.18893945T= , CM000681.1:g.18893945T=	GRCh37
NC_000019.8:g.18754945T=	NCBI36
NG_007070.1:g.13170A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.2146A= MANE Select	ENSP00000222271.2:p.Thr716=
ENST00000222271.6:c.2146A=	ENSP00000222271.2:p.Thr716=
ENST00000425807.1:c.1987A=	ENSP00000403792.1:p.Thr663=
ENST00000542601.6:c.2047A=	ENSP00000439156.2:p.Thr683=
NM_000095.2:c.2146A=	NP_000086.2:p.Thr716=
NM_000095.3:c.2146A= MANE Select	NP_000086.2:p.Thr716=