Canonical Allele Identifier: CA404882124

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896494C>T (hg19) ; chr19:g.18785684C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785684C>T , CM000681.2:g.18785684C>T	GRCh38
NC_000019.9:g.18896494C>T , CM000681.1:g.18896494C>T	GRCh37
NC_000019.8:g.18757494C>T	NCBI36
NG_007070.1:g.10621G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1657G>A MANE Select	ENSP00000222271.2:p.Val553Met
ENST00000222271.6:c.1657G>A	ENSP00000222271.2:p.Val553Met
ENST00000425807.1:c.1498G>A	ENSP00000403792.1:p.Val500Met
ENST00000542601.6:c.1558G>A	ENSP00000439156.2:p.Val520Met
NM_000095.2:c.1657G>A	NP_000086.2:p.Val553Met
NM_000095.3:c.1657G>A MANE Select	NP_000086.2:p.Val553Met