Canonical Allele Identifier: CA1784506207
Gene: OPRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.53240422T= , CM000670.2:g.53240422T= GRCh38
NC_000008.10:g.54152982T= , CM000670.1:g.54152982T= GRCh37
NC_000008.9:g.54315535T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265572.8:c.258-5311A= MANE Select ENSP00000265572.3:n.258-5311A=
ENST00000673285.2:c.258-5311A= ENSP00000500765.2:n.258-5311A=
ENST00000265572.7:c.258-5311A= ENSP00000265572.3:n.258-5311A=
ENST00000520287.5:c.258-5311A= ENSP00000429706.1:n.258-5311A=
ENST00000522508.1:c.*80+2317A= ENSP00000428231.1:n.*80+2317A=
ENST00000612786.4:c.-11+2317A= ENSP00000483000.1:n.-11+2317A=
ENST00000613482.1:c.216-5311A= ENSP00000478453.1:n.216-5311A=
NM_000912.3:c.258-5311A= NP_000903.2:n.258-5311A=
NM_001282904.1:c.-11+2317A= NP_001269833.1:n.-11+2317A=
NM_000912.4:c.258-5311A= NP_000903.2:n.258-5311A=
NM_001318497.1:c.258-5311A= NP_001305426.1:n.258-5311A=
NM_000912.5:c.258-5311A= MANE Select NP_000903.2:n.258-5311A=
NM_001318497.2:c.258-5311A= NP_001305426.1:n.258-5311A=
NM_001282904.2:c.-11+2317A= NP_001269833.1:n.-11+2317A=