Canonical Allele Identifier: CA1752388284

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861127A= , CM000669.2:g.150861127A=	GRCh38
NC_000007.13:g.150558215A= , CM000669.1:g.150558215A=	GRCh37
NC_000007.12:g.150189148A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360937.9:c.2174A= MANE Select	ENSP00000354193.4:p.Tyr725=
ENST00000360937.8:c.2174A=	ENSP00000354193.4:p.Tyr725=
ENST00000416793.6:c.2231A=	ENSP00000411613.2:p.Tyr744=
ENST00000467291.5:c.2174A=	ENSP00000418328.1:p.Tyr725=
ENST00000480582.1:n.851A=
ENST00000493429.5:c.2174A=	ENSP00000418614.1:p.Tyr725=
ENST00000619575.1:c.*31A=	ENSP00000481717.1:n.*31A=
ENST00000622116.4:c.*166A=	ENSP00000481520.1:n.*166A=
NM_001091.3:c.2174A=	NP_001082.2:p.Tyr725=
NM_001272072.1:c.2231A=	NP_001259001.1:p.Tyr744=
XM_011516008.1:c.2231A=	XP_011514310.1:p.Tyr744=
XM_011516009.1:c.2174A=	XP_011514311.1:p.Tyr725=
XR_928169.1:n.295+15882T=
XR_928170.1:n.425+7489T=
XR_928171.1:n.297+15882T=
XM_017011944.1:c.2231A=	XP_016867433.1:p.Tyr744=
XM_017011945.1:c.2231A=	XP_016867434.1:p.Tyr744=
XM_017011946.2:c.2231A=	XP_016867435.1:p.Tyr744=
XM_017011947.1:c.2174A=	XP_016867436.1:p.Tyr725=
XR_928169.2:n.301+15882T=
XR_928171.2:n.301+15882T=
NM_001091.4:c.2174A= MANE Select	NP_001082.2:p.Tyr725=
NM_001272072.2:c.2231A=	NP_001259001.1:p.Tyr744=