Canonical Allele Identifier: CA2580596232
Gene: OPRK1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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