Canonical Allele Identifier: CA404879286

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18895888T>C (hg19) ; chr19:g.18785078T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785078T>C , CM000681.2:g.18785078T>C	GRCh38
NC_000019.9:g.18895888T>C , CM000681.1:g.18895888T>C	GRCh37
NC_000019.8:g.18756888T>C	NCBI36
NG_007070.1:g.11227A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1732A>G MANE Select	ENSP00000222271.2:p.Asn578Asp
ENST00000222271.6:c.1732A>G	ENSP00000222271.2:p.Asn578Asp
ENST00000425807.1:c.1573A>G	ENSP00000403792.1:p.Asn525Asp
ENST00000542601.6:c.1633A>G	ENSP00000439156.2:p.Asn545Asp
NM_000095.2:c.1732A>G	NP_000086.2:p.Asn578Asp
NM_000095.3:c.1732A>G MANE Select	NP_000086.2:p.Asn578Asp