Canonical Allele Identifier: CA2580593793
Community Standard Title: NM_000914.5(OPRM1):c.*2109A>C
Gene: OPRM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154120830A>C , CM000668.2:g.154120830A>C GRCh38
NC_000006.11:g.154441965A>C , CM000668.1:g.154441965A>C GRCh37
NC_000006.10:g.154483657A>C NCBI36
NG_021208.1:g.115330A>C
NG_021208.2:g.115330A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000914.5:c.*2109A>C MANE Select NP_000905.3:n.*2109A>C
ENST00000330432.12:c.*2109A>C MANE Select ENSP00000328264.7:n.*2109A>C
NM_000914.4:c.*2109A>C NP_000905.3:n.*2109A>C
NM_001008503.2:c.1164+29358A>C NP_001008503.2:n.1164+29358A>C
NM_001008503.3:c.1164+29358A>C NP_001008503.2:n.1164+29358A>C
NM_001145279.3:c.*2109A>C NP_001138751.1:n.*2109A>C
NM_001145279.4:c.*2109A>C NP_001138751.1:n.*2109A>C
NM_001145280.3:c.*2109A>C NP_001138752.1:n.*2109A>C
NM_001145280.4:c.*2109A>C NP_001138752.1:n.*2109A>C
NM_001145281.2:c.*2109A>C NP_001138753.1:n.*2109A>C
NM_001145281.3:c.*2109A>C NP_001138753.1:n.*2109A>C
NM_001145287.2:c.*2109A>C NP_001138759.1:n.*2109A>C
NM_001145287.3:c.*2109A>C NP_001138759.1:n.*2109A>C
NM_001285522.1:c.*2144A>C NP_001272451.1:n.*2144A>C
NM_001285524.1:c.*2109A>C NP_001272453.1:n.*2109A>C
NM_001285526.1:c.*2109A>C NP_001272455.1:n.*2109A>C
NM_001285526.2:c.*2109A>C NP_001272455.1:n.*2109A>C
NR_104348.1:n.3555A>C
NR_104350.1:n.3093A>C
ENST00000337049.8:c.1164+29358A>C ENSP00000338381.4:n.1164+29358A>C
ENST00000524150.2:c.*250+29358A>C ENSP00000430575.1:n.*250+29358A>C
XM_011535849.1:c.*293-191A>C XP_011534151.1:n.*293-191A>C
XM_011535859.1:c.*2109A>C XP_011534161.1:n.*2109A>C
XM_011535860.1:c.*2109A>C XP_011534162.1:n.*2109A>C
XM_011535861.1:c.*2109A>C XP_011534163.1:n.*2109A>C
XM_017010906.2:c.*2109A>C XP_016866395.1:n.*2109A>C