Canonical Allele Identifier: CA404885330

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896951C>T (hg19) ; chr19:g.18786141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786141C>T , CM000681.2:g.18786141C>T	GRCh38
NC_000019.9:g.18896951C>T , CM000681.1:g.18896951C>T	GRCh37
NC_000019.8:g.18757951C>T	NCBI36
NG_007070.1:g.10164G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1313G>A MANE Select	ENSP00000222271.2:p.Gly438Glu
ENST00000222271.6:c.1313G>A	ENSP00000222271.2:p.Gly438Glu
ENST00000425807.1:c.1154G>A	ENSP00000403792.1:p.Gly385Glu
ENST00000542601.6:c.1214G>A	ENSP00000439156.2:p.Gly405Glu
ENST00000612179.1:n.563G>A
NM_000095.2:c.1313G>A	NP_000086.2:p.Gly438Glu
NM_000095.3:c.1313G>A MANE Select	NP_000086.2:p.Gly438Glu