Canonical Allele Identifier: CA1752388293
Gene: AOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861130T= , CM000669.2:g.150861130T= GRCh38
NC_000007.13:g.150558218T= , CM000669.1:g.150558218T= GRCh37
NC_000007.12:g.150189151T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360937.9:c.2177T= MANE Select ENSP00000354193.4:p.Val726=
ENST00000360937.8:c.2177T= ENSP00000354193.4:p.Val726=
ENST00000416793.6:c.2234T= ENSP00000411613.2:p.Val745=
ENST00000467291.5:c.2177T= ENSP00000418328.1:p.Val726=
ENST00000480582.1:n.854T=
ENST00000493429.5:c.2177T= ENSP00000418614.1:p.Val726=
ENST00000619575.1:c.*34T= ENSP00000481717.1:n.*34T=
ENST00000622116.4:c.*169T= ENSP00000481520.1:n.*169T=
NM_001091.3:c.2177T= NP_001082.2:p.Val726=
NM_001272072.1:c.2234T= NP_001259001.1:p.Val745=
XM_011516008.1:c.2234T= XP_011514310.1:p.Val745=
XM_011516009.1:c.2177T= XP_011514311.1:p.Val726=
XR_928169.1:n.295+15879A=
XR_928170.1:n.425+7486A=
XR_928171.1:n.297+15879A=
XM_017011944.1:c.2234T= XP_016867433.1:p.Val745=
XM_017011945.1:c.2234T= XP_016867434.1:p.Val745=
XM_017011946.2:c.2234T= XP_016867435.1:p.Val745=
XM_017011947.1:c.2177T= XP_016867436.1:p.Val726=
XR_928169.2:n.301+15879A=
XR_928171.2:n.301+15879A=
NM_001091.4:c.2177T= MANE Select NP_001082.2:p.Val726=
NM_001272072.2:c.2234T= NP_001259001.1:p.Val745=