Canonical Allele Identifier: CA369846186
Gene: AOC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150856724T>A , CM000669.2:g.150856724T>A GRCh38
NC_000007.13:g.150553812T>A , CM000669.1:g.150553812T>A GRCh37
NC_000007.12:g.150184745T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.254T>A MANE Select ENSP00000354193.4:p.Phe85Tyr
ENST00000360937.8:c.254T>A ENSP00000354193.4:p.Phe85Tyr
ENST00000416793.6:c.254T>A ENSP00000411613.2:p.Phe85Tyr
ENST00000460213.1:c.254T>A ENSP00000418557.1:p.Phe85Tyr
ENST00000467291.5:c.254T>A ENSP00000418328.1:p.Phe85Tyr
ENST00000483043.1:c.254T>A ENSP00000417392.1:p.Phe85Tyr
ENST00000493429.5:c.254T>A ENSP00000418614.1:p.Phe85Tyr
ENST00000619575.1:c.254T>A ENSP00000481717.1:p.Phe85Tyr
ENST00000622116.4:c.-1169T>A ENSP00000481520.1:n.-1169T>A
NM_001091.3:c.254T>A NP_001082.2:p.Phe85Tyr
NM_001272072.1:c.254T>A NP_001259001.1:p.Phe85Tyr
XM_011516008.1:c.254T>A XP_011514310.1:p.Phe85Tyr
XM_011516009.1:c.254T>A XP_011514311.1:p.Phe85Tyr
XR_928169.1:n.296-15279A>T
XR_928170.1:n.425+11892A>T
XR_928171.1:n.298-15279A>T
XM_017011944.1:c.254T>A XP_016867433.1:p.Phe85Tyr
XM_017011945.1:c.254T>A XP_016867434.1:p.Phe85Tyr
XM_017011946.2:c.254T>A XP_016867435.1:p.Phe85Tyr
XM_017011947.1:c.254T>A XP_016867436.1:p.Phe85Tyr
XR_928169.2:n.302-15279A>T
XR_928171.2:n.302-15279A>T
NM_001091.4:c.254T>A MANE Select NP_001082.2:p.Phe85Tyr
NM_001272072.2:c.254T>A NP_001259001.1:p.Phe85Tyr