Canonical Allele Identifier: CA404884729
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786061C>G , CM000681.2:g.18786061C>G GRCh38
NC_000019.9:g.18896871C>G , CM000681.1:g.18896871C>G GRCh37
NC_000019.8:g.18757871C>G NCBI36
NG_007070.1:g.10244G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1393G>C MANE Select ENSP00000222271.2:p.Gly465Arg
ENST00000222271.6:c.1393G>C ENSP00000222271.2:p.Gly465Arg
ENST00000425807.1:c.1234G>C ENSP00000403792.1:p.Gly412Arg
ENST00000542601.6:c.1294G>C ENSP00000439156.2:p.Gly432Arg
NM_000095.2:c.1393G>C NP_000086.2:p.Gly465Arg
NM_000095.3:c.1393G>C MANE Select NP_000086.2:p.Gly465Arg