Canonical Allele Identifier: CA366152344

Gene: OPRM1

Linked Data

• dbSNP Id: rs1457556221
• gnomAD v2: 6-154360720-C-G
• gnomAD v4: 6-154039585-C-G
• MyVariant Identifiers: chr6:g.154360720C>G (hg19) ; chr6:g.154039585C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039585C>G , CM000668.2:g.154039585C>G	GRCh38
NC_000006.11:g.154360720C>G , CM000668.1:g.154360720C>G	GRCh37
NC_000006.10:g.154402413C>G	NCBI36
NG_021208.1:g.34085C>G
NG_021208.2:g.34085C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000330432.12:c.41C>G MANE Select	ENSP00000328264.7:p.Thr14Ser
ENST00000229768.9:c.41C>G	ENSP00000229768.5:p.Thr14Ser
ENST00000330432.11:c.41C>G	ENSP00000328264.7:p.Thr14Ser
ENST00000337049.8:c.41C>G	ENSP00000338381.4:p.Thr14Ser
ENST00000360422.8:c.227C>G	ENSP00000353598.5:p.Thr76Ser
ENST00000414028.6:c.41C>G	ENSP00000399359.2:p.Thr14Ser
ENST00000419506.6:c.41C>G	ENSP00000403549.2:p.Thr14Ser
ENST00000428397.6:c.41C>G	ENSP00000411903.2:p.Thr14Ser
ENST00000434900.6:c.320C>G	ENSP00000394624.2:p.Thr107Ser
ENST00000435918.6:c.41C>G	ENSP00000413752.2:p.Thr14Ser
ENST00000452687.6:c.41C>G	ENSP00000410497.2:p.Thr14Ser
ENST00000518759.5:c.47+29026C>G	ENSP00000430260.1:n.47+29026C>G
ENST00000519083.5:c.41C>G	ENSP00000431048.1:p.Thr14Ser
ENST00000520282.5:c.185C>G	ENSP00000430247.1:p.Thr62Ser
ENST00000520708.5:c.-11+28567C>G	ENSP00000430876.1:n.-11+28567C>G
ENST00000522739.5:c.41C>G	ENSP00000428018.1:p.Thr14Ser
ENST00000523520.1:n.222C>G
ENST00000524150.2:c.41C>G	ENSP00000430575.1:p.Thr14Ser
ENST00000524163.5:c.41C>G	ENSP00000430097.1:p.Thr14Ser
NM_000914.4:c.41C>G	NP_000905.3:p.Thr14Ser
NM_001008503.2:c.41C>G	NP_001008503.2:p.Thr14Ser
NM_001008504.3:c.41C>G	NP_001008504.2:p.Thr14Ser
NM_001008505.2:c.41C>G	NP_001008505.2:p.Thr14Ser
NM_001145279.3:c.320C>G	NP_001138751.1:p.Thr107Ser
NM_001145280.3:c.-11+28567C>G	NP_001138752.1:n.-11+28567C>G
NM_001145281.2:c.47+29026C>G	NP_001138753.1:n.47+29026C>G
NM_001145282.2:c.41C>G	NP_001138754.1:p.Thr14Ser
NM_001145283.2:c.41C>G	NP_001138755.1:p.Thr14Ser
NM_001145284.3:c.41C>G	NP_001138756.1:p.Thr14Ser
NM_001145285.2:c.41C>G	NP_001138757.1:p.Thr14Ser
NM_001145286.2:c.41C>G	NP_001138758.1:p.Thr14Ser
NM_001285522.1:c.41C>G	NP_001272451.1:p.Thr14Ser
NM_001285523.1:c.41C>G	NP_001272452.1:p.Thr14Ser
NM_001285524.1:c.320C>G	NP_001272453.1:p.Thr107Ser
NR_104348.1:n.175C>G
NR_104349.1:n.175C>G
NR_104350.1:n.175C>G
NR_104351.1:n.175C>G
XM_006715497.2:c.227C>G	XP_006715560.1:p.Thr76Ser
XM_011535849.1:c.320C>G	XP_011534151.1:p.Thr107Ser
NM_001285523.2:c.41C>G	NP_001272452.1:p.Thr14Ser
XM_017010907.2:c.227C>G	XP_016866396.1:p.Thr76Ser
NM_000914.5:c.41C>G MANE Select	NP_000905.3:p.Thr14Ser
NM_001008503.3:c.41C>G	NP_001008503.2:p.Thr14Ser
NM_001008504.4:c.41C>G	NP_001008504.2:p.Thr14Ser
NM_001145279.4:c.320C>G	NP_001138751.1:p.Thr107Ser
NM_001145280.4:c.-11+28567C>G	NP_001138752.1:n.-11+28567C>G
NM_001145281.3:c.47+29026C>G	NP_001138753.1:n.47+29026C>G
NM_001145285.3:c.41C>G	NP_001138757.1:p.Thr14Ser
NM_001145286.3:c.41C>G	NP_001138758.1:p.Thr14Ser
NM_001285523.3:c.41C>G	NP_001272452.1:p.Thr14Ser