Canonical Allele Identifier: CA1752395514
Gene: AOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150857145C= , CM000669.2:g.150857145C= GRCh38
NC_000007.13:g.150554233C= , CM000669.1:g.150554233C= GRCh37
NC_000007.12:g.150185166C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.675C= MANE Select ENSP00000354193.4:p.Ser225=
ENST00000360937.8:c.675C= ENSP00000354193.4:p.Ser225=
ENST00000416793.6:c.675C= ENSP00000411613.2:p.Ser225=
ENST00000460213.1:c.675C= ENSP00000418557.1:p.Ser225=
ENST00000467291.5:c.675C= ENSP00000418328.1:p.Ser225=
ENST00000483043.1:c.675C= ENSP00000417392.1:p.Ser225=
ENST00000493429.5:c.675C= ENSP00000418614.1:p.Ser225=
ENST00000619575.1:c.675C= ENSP00000481717.1:p.Ser225=
ENST00000622116.4:c.-748C= ENSP00000481520.1:n.-748C=
NM_001091.3:c.675C= NP_001082.2:p.Ser225=
NM_001272072.1:c.675C= NP_001259001.1:p.Ser225=
XM_011516008.1:c.675C= XP_011514310.1:p.Ser225=
XM_011516009.1:c.675C= XP_011514311.1:p.Ser225=
XR_928169.1:n.296-15700G=
XR_928170.1:n.425+11471G=
XR_928171.1:n.298-15700G=
XM_017011944.1:c.675C= XP_016867433.1:p.Ser225=
XM_017011945.1:c.675C= XP_016867434.1:p.Ser225=
XM_017011946.2:c.675C= XP_016867435.1:p.Ser225=
XM_017011947.1:c.675C= XP_016867436.1:p.Ser225=
XR_928169.2:n.302-15700G=
XR_928171.2:n.302-15700G=
NM_001091.4:c.675C= MANE Select NP_001082.2:p.Ser225=
NM_001272072.2:c.675C= NP_001259001.1:p.Ser225=