Canonical Allele Identifier: CA1752388392

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861198A= , CM000669.2:g.150861198A=	GRCh38
NC_000007.13:g.150558286A= , CM000669.1:g.150558286A=	GRCh37
NC_000007.12:g.150189219A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.2245A= MANE Select	ENSP00000354193.4:p.Arg749=
ENST00000360937.8:c.2245A=	ENSP00000354193.4:p.Arg749=
ENST00000416793.6:c.2302A=	ENSP00000411613.2:p.Arg768=
ENST00000467291.5:c.2245A=	ENSP00000418328.1:p.Arg749=
ENST00000480582.1:n.922A=
ENST00000493429.5:c.2245A=	ENSP00000418614.1:p.Arg749=
ENST00000619575.1:c.*102A=	ENSP00000481717.1:n.*102A=
ENST00000622116.4:c.*237A=	ENSP00000481520.1:n.*237A=
NM_001091.3:c.2245A=	NP_001082.2:p.Arg749=
NM_001272072.1:c.2302A=	NP_001259001.1:p.Arg768=
XM_011516008.1:c.2302A=	XP_011514310.1:p.Arg768=
XM_011516009.1:c.2245A=	XP_011514311.1:p.Arg749=
XR_928169.1:n.295+15811T=
XR_928170.1:n.425+7418T=
XR_928171.1:n.297+15811T=
XM_017011944.1:c.2302A=	XP_016867433.1:p.Arg768=
XM_017011945.1:c.2302A=	XP_016867434.1:p.Arg768=
XM_017011946.2:c.2302A=	XP_016867435.1:p.Arg768=
XM_017011947.1:c.2245A=	XP_016867436.1:p.Arg749=
XR_928169.2:n.301+15811T=
XR_928171.2:n.301+15811T=
NM_001091.4:c.2245A= MANE Select	NP_001082.2:p.Arg749=
NM_001272072.2:c.2302A=	NP_001259001.1:p.Arg768=