Canonical Allele Identifier: CA1752395729
Gene: AOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150857269C= , CM000669.2:g.150857269C= GRCh38
NC_000007.13:g.150554357C= , CM000669.1:g.150554357C= GRCh37
NC_000007.12:g.150185290C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.799C= MANE Select ENSP00000354193.4:p.Leu267=
ENST00000360937.8:c.799C= ENSP00000354193.4:p.Leu267=
ENST00000416793.6:c.799C= ENSP00000411613.2:p.Leu267=
ENST00000467291.5:c.799C= ENSP00000418328.1:p.Leu267=
ENST00000483043.1:c.799C= ENSP00000417392.1:p.Leu267=
ENST00000493429.5:c.799C= ENSP00000418614.1:p.Leu267=
ENST00000619575.1:c.798C= ENSP00000481717.1:p.Arg266=
ENST00000622116.4:c.-624C= ENSP00000481520.1:n.-624C=
NM_001091.3:c.799C= NP_001082.2:p.Leu267=
NM_001272072.1:c.799C= NP_001259001.1:p.Leu267=
XM_011516008.1:c.799C= XP_011514310.1:p.Leu267=
XM_011516009.1:c.799C= XP_011514311.1:p.Leu267=
XR_928169.1:n.296-15824G=
XR_928170.1:n.425+11347G=
XR_928171.1:n.298-15824G=
XM_017011944.1:c.799C= XP_016867433.1:p.Leu267=
XM_017011945.1:c.799C= XP_016867434.1:p.Leu267=
XM_017011946.2:c.799C= XP_016867435.1:p.Leu267=
XM_017011947.1:c.799C= XP_016867436.1:p.Leu267=
XR_928169.2:n.302-15824G=
XR_928171.2:n.302-15824G=
NM_001091.4:c.799C= MANE Select NP_001082.2:p.Leu267=
NM_001272072.2:c.799C= NP_001259001.1:p.Leu267=