Canonical Allele Identifier: CA1161091765
Gene: OPRD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28834925C= , CM000663.2:g.28834925C= GRCh38
NC_000001.10:g.29161437C= , CM000663.1:g.29161437C= GRCh37
NC_000001.9:g.29034024C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234961.7:c.227+22315C= MANE Select ENSP00000234961.2:n.227+22315C=
ENST00000234961.6:c.227+22315C= ENSP00000234961.2:n.227+22315C=
ENST00000621425.1:c.227+22315C= ENSP00000477970.1:n.227+22315C=
NM_000911.3:c.227+22315C= NP_000902.3:n.227+22315C=
NM_000911.4:c.227+22315C= MANE Select NP_000902.3:n.227+22315C=