Canonical Allele Identifier: CA1752396498

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150857537T= , CM000669.2:g.150857537T=	GRCh38
NC_000007.13:g.150554625T= , CM000669.1:g.150554625T=	GRCh37
NC_000007.12:g.150185558T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.1067T= MANE Select	ENSP00000354193.4:p.Val356=
ENST00000360937.8:c.1067T=	ENSP00000354193.4:p.Val356=
ENST00000416793.6:c.1067T=	ENSP00000411613.2:p.Val356=
ENST00000467291.5:c.1067T=	ENSP00000418328.1:p.Val356=
ENST00000493429.5:c.1067T=	ENSP00000418614.1:p.Val356=
ENST00000619575.1:c.1064T=	ENSP00000481717.1:p.Val355=
ENST00000622116.4:c.-356T=	ENSP00000481520.1:n.-356T=
NM_001091.3:c.1067T=	NP_001082.2:p.Val356=
NM_001272072.1:c.1067T=	NP_001259001.1:p.Val356=
XM_011516008.1:c.1067T=	XP_011514310.1:p.Val356=
XM_011516009.1:c.1067T=	XP_011514311.1:p.Val356=
XR_928169.1:n.296-16092A=
XR_928170.1:n.425+11079A=
XR_928171.1:n.298-16092A=
XM_017011944.1:c.1067T=	XP_016867433.1:p.Val356=
XM_017011945.1:c.1067T=	XP_016867434.1:p.Val356=
XM_017011946.2:c.1067T=	XP_016867435.1:p.Val356=
XM_017011947.1:c.1067T=	XP_016867436.1:p.Val356=
XR_928169.2:n.302-16092A=
XR_928171.2:n.302-16092A=
NM_001091.4:c.1067T= MANE Select	NP_001082.2:p.Val356=
NM_001272072.2:c.1067T=	NP_001259001.1:p.Val356=