Canonical Allele Identifier: CA1752388412

Gene: AOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150861218C= , CM000669.2:g.150861218C=	GRCh38
NC_000007.13:g.150558306C= , CM000669.1:g.150558306C=	GRCh37
NC_000007.12:g.150189239C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360937.9:c.*9C= MANE Select	ENSP00000354193.4:n.*9C=
ENST00000360937.8:c.*9C=	ENSP00000354193.4:n.*9C=
ENST00000416793.6:c.*9C=	ENSP00000411613.2:n.*9C=
ENST00000467291.5:c.*9C=	ENSP00000418328.1:n.*9C=
ENST00000480582.1:n.942C=
ENST00000493429.5:c.*9C=	ENSP00000418614.1:n.*9C=
ENST00000619575.1:c.*122C=	ENSP00000481717.1:n.*122C=
ENST00000622116.4:c.*257C=	ENSP00000481520.1:n.*257C=
NM_001091.3:c.*9C=	NP_001082.2:n.*9C=
NM_001272072.1:c.*9C=	NP_001259001.1:n.*9C=
XM_011516008.1:c.*9C=	XP_011514310.1:n.*9C=
XM_011516009.1:c.*9C=	XP_011514311.1:n.*9C=
XR_928169.1:n.295+15791G=
XR_928170.1:n.425+7398G=
XR_928171.1:n.297+15791G=
XM_017011944.1:c.*9C=	XP_016867433.1:n.*9C=
XM_017011945.1:c.*9C=	XP_016867434.1:n.*9C=
XM_017011946.2:c.*9C=	XP_016867435.1:n.*9C=
XM_017011947.1:c.*9C=	XP_016867436.1:n.*9C=
XR_928169.2:n.301+15791G=
XR_928171.2:n.301+15791G=
NM_001091.4:c.*9C= MANE Select	NP_001082.2:n.*9C=
NM_001272072.2:c.*9C=	NP_001259001.1:n.*9C=