Canonical Allele Identifier: CA404877805

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18895724C>A (hg19) ; chr19:g.18784914C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18784914C>A , CM000681.2:g.18784914C>A	GRCh38
NC_000019.9:g.18895724C>A , CM000681.1:g.18895724C>A	GRCh37
NC_000019.8:g.18756724C>A	NCBI36
NG_007070.1:g.11391G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1896G>T MANE Select	ENSP00000222271.2:p.Glu632Asp
ENST00000222271.6:c.1896G>T	ENSP00000222271.2:p.Glu632Asp
ENST00000425807.1:c.1737G>T	ENSP00000403792.1:p.Glu579Asp
ENST00000542601.6:c.1797G>T	ENSP00000439156.2:p.Glu599Asp
NM_000095.2:c.1896G>T	NP_000086.2:p.Glu632Asp
NM_000095.3:c.1896G>T MANE Select	NP_000086.2:p.Glu632Asp