Canonical Allele Identifier: CA1784495221
Gene: OPRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.53229264C= , CM000670.2:g.53229264C= GRCh38
NC_000008.10:g.54141824C= , CM000670.1:g.54141824C= GRCh37
NC_000008.9:g.54304377C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265572.8:c.*33G= MANE Select ENSP00000265572.3:n.*33G=
ENST00000673285.2:c.1176G= ENSP00000500765.2:p.Ser392=
ENST00000265572.7:c.*33G= ENSP00000265572.3:n.*33G=
ENST00000520287.5:c.*33G= ENSP00000429706.1:n.*33G=
ENST00000522508.1:c.*999G= ENSP00000428231.1:n.*999G=
ENST00000524278.5:c.*33G= ENSP00000430923.1:n.*33G=
ENST00000612786.4:c.*33G= ENSP00000483000.1:n.*33G=
ENST00000613482.1:c.1134G= ENSP00000478453.1:n.1134G=
NM_000912.3:c.*33G= NP_000903.2:n.*33G=
NM_001282904.1:c.*33G= NP_001269833.1:n.*33G=
NM_000912.4:c.*33G= NP_000903.2:n.*33G=
NM_001318497.1:c.1176G= NP_001305426.1:p.Ser392=
NM_000912.5:c.*33G= MANE Select NP_000903.2:n.*33G=
NM_001318497.2:c.1176G= NP_001305426.1:p.Ser392=
NM_001282904.2:c.*33G= NP_001269833.1:n.*33G=