Canonical Allele Identifier: CA404885628
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786245T>C , CM000681.2:g.18786245T>C GRCh38
NC_000019.9:g.18897055T>C , CM000681.1:g.18897055T>C GRCh37
NC_000019.8:g.18758055T>C NCBI36
NG_007070.1:g.10060A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1301A>G MANE Select ENSP00000222271.2:p.Gln434Arg
ENST00000222271.6:c.1301A>G ENSP00000222271.2:p.Gln434Arg
ENST00000425807.1:c.1142A>G ENSP00000403792.1:p.Gln381Arg
ENST00000542601.6:c.1202A>G ENSP00000439156.2:p.Gln401Arg
ENST00000612179.1:n.551A>G
NM_000095.2:c.1301A>G NP_000086.2:p.Gln434Arg
NM_000095.3:c.1301A>G MANE Select NP_000086.2:p.Gln434Arg