Canonical Allele Identifier: CA404879169

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18895877G>C (hg19) ; chr19:g.18785067G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785067G>C , CM000681.2:g.18785067G>C	GRCh38
NC_000019.9:g.18895877G>C , CM000681.1:g.18895877G>C	GRCh37
NC_000019.8:g.18756877G>C	NCBI36
NG_007070.1:g.11238C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1743C>G MANE Select	ENSP00000222271.2:p.Asp581Glu
ENST00000222271.6:c.1743C>G	ENSP00000222271.2:p.Asp581Glu
ENST00000425807.1:c.1584C>G	ENSP00000403792.1:p.Asp528Glu
ENST00000542601.6:c.1644C>G	ENSP00000439156.2:p.Asp548Glu
NM_000095.2:c.1743C>G	NP_000086.2:p.Asp581Glu
NM_000095.3:c.1743C>G MANE Select	NP_000086.2:p.Asp581Glu