Canonical Allele Identifier: CA404896588

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18900075C>G (hg19) ; chr19:g.18789266C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789266C>G , CM000681.2:g.18789266C>G	GRCh38
NC_000019.9:g.18900075C>G , CM000681.1:g.18900075C>G	GRCh37
NC_000019.8:g.18761075C>G	NCBI36
NG_007070.1:g.7040G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.422G>C MANE Select	ENSP00000222271.2:p.Arg141Pro
ENST00000222271.6:c.422G>C	ENSP00000222271.2:p.Arg141Pro
ENST00000425807.1:c.391-374G>C	ENSP00000403792.1:n.391-374G>C
ENST00000542601.6:c.323G>C	ENSP00000439156.2:p.Arg108Pro
NM_000095.2:c.422G>C	NP_000086.2:p.Arg141Pro
NM_000095.3:c.422G>C MANE Select	NP_000086.2:p.Arg141Pro