Canonical Allele Identifier: CA1752395658

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150857236G= , CM000669.2:g.150857236G=	GRCh38
NC_000007.13:g.150554324G= , CM000669.1:g.150554324G=	GRCh37
NC_000007.12:g.150185257G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.766G= MANE Select	ENSP00000354193.4:p.Gly256=
ENST00000360937.8:c.766G=	ENSP00000354193.4:p.Gly256=
ENST00000416793.6:c.766G=	ENSP00000411613.2:p.Gly256=
ENST00000467291.5:c.766G=	ENSP00000418328.1:p.Gly256=
ENST00000483043.1:c.766G=	ENSP00000417392.1:p.Gly256=
ENST00000493429.5:c.766G=	ENSP00000418614.1:p.Gly256=
ENST00000619575.1:c.766G=	ENSP00000481717.1:p.Gly256=
ENST00000622116.4:c.-657G=	ENSP00000481520.1:n.-657G=
NM_001091.3:c.766G=	NP_001082.2:p.Gly256=
NM_001272072.1:c.766G=	NP_001259001.1:p.Gly256=
XM_011516008.1:c.766G=	XP_011514310.1:p.Gly256=
XM_011516009.1:c.766G=	XP_011514311.1:p.Gly256=
XR_928169.1:n.296-15791C=
XR_928170.1:n.425+11380C=
XR_928171.1:n.298-15791C=
XM_017011944.1:c.766G=	XP_016867433.1:p.Gly256=
XM_017011945.1:c.766G=	XP_016867434.1:p.Gly256=
XM_017011946.2:c.766G=	XP_016867435.1:p.Gly256=
XM_017011947.1:c.766G=	XP_016867436.1:p.Gly256=
XR_928169.2:n.302-15791C=
XR_928171.2:n.302-15791C=
NM_001091.4:c.766G= MANE Select	NP_001082.2:p.Gly256=
NM_001272072.2:c.766G=	NP_001259001.1:p.Gly256=