Canonical Allele Identifier: CA506117388

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896552G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785742G>T , CM000681.2:g.18785742G>T	GRCh38
NC_000019.9:g.18896552G>T , CM000681.1:g.18896552G>T	GRCh37
NC_000019.8:g.18757552G>T	NCBI36
NG_007070.1:g.10563C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1599C>A MANE Select	ENSP00000222271.2:p.Ala533=
ENST00000222271.6:c.1599C>A	ENSP00000222271.2:p.Ala533=
ENST00000425807.1:c.1440C>A	ENSP00000403792.1:p.Ala480=
ENST00000542601.6:c.1500C>A	ENSP00000439156.2:p.Ala500=
NM_000095.2:c.1599C>A	NP_000086.2:p.Ala533=
NM_000095.3:c.1599C>A MANE Select	NP_000086.2:p.Ala533=