Canonical Allele Identifier: CA409768796

Gene: OPRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.64098146T>G , CM000682.2:g.64098146T>G	GRCh38
NC_000020.10:g.62729499T>G , CM000682.1:g.62729499T>G	GRCh37
NC_000020.9:g.62199943T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_182647.4:c.578T>G MANE Select	NP_872588.1:p.Val193Gly
ENST00000336866.7:c.578T>G MANE Select	ENSP00000336843.2:p.Val193Gly
NM_000913.4:c.578T>G	NP_000904.1:p.Val193Gly
NM_000913.5:c.578T>G	NP_000904.1:p.Val193Gly
NM_000913.6:c.578T>G	NP_000904.1:p.Val193Gly
NM_001200019.1:c.578T>G	NP_001186948.1:p.Val193Gly
NM_001200019.2:c.578T>G	NP_001186948.1:p.Val193Gly
NM_001318853.1:c.578T>G	NP_001305782.1:p.Val193Gly
NM_001318853.2:c.578T>G	NP_001305782.1:p.Val193Gly
NM_001318854.1:c.563T>G	NP_001305783.1:p.Val188Gly
NM_001318855.1:c.491T>G	NP_001305784.1:p.Val164Gly
NM_182647.2:c.578T>G	NP_872588.1:p.Val193Gly
NM_182647.3:c.578T>G	NP_872588.1:p.Val193Gly
ENST00000336866.6:c.578T>G	ENSP00000336843.2:p.Val193Gly
ENST00000349451.3:c.578T>G	ENSP00000336764.3:p.Val193Gly
ENST00000355631.8:c.578T>G	ENSP00000347848.4:p.Val193Gly
ENST00000672146.2:c.578T>G	ENSP00000500894.2:p.Val193Gly
ENST00000672146.3:c.578T>G	ENSP00000500894.2:p.Val193Gly
XM_011528828.1:c.632T>G	XP_011527130.1:p.Val211Gly
XM_011528828.3:c.632T>G	XP_011527130.1:p.Val211Gly
XM_011528829.1:c.617T>G	XP_011527131.1:p.Val206Gly
XM_011528830.1:c.335T>G	XP_011527132.1:p.Val112Gly
XM_011528830.3:c.335T>G	XP_011527132.1:p.Val112Gly
XM_017027853.1:c.632T>G	XP_016883342.1:p.Val211Gly
XM_017027854.1:c.578T>G	XP_016883343.1:p.Val193Gly
XM_017027855.1:c.563T>G	XP_016883344.1:p.Val188Gly