Canonical Allele Identifier: CA2716185034
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs2116832835

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150857386dup , CM000669.2:g.150857386dup GRCh38
NC_000007.13:g.150554474dup , CM000669.1:g.150554474dup GRCh37
NC_000007.12:g.150185407dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.916dup MANE Select ENSP00000354193.4:p.His306ProfsTer?
ENST00000360937.8:c.916dup ENSP00000354193.4:p.His306ProfsTer?
ENST00000416793.6:c.916dup ENSP00000411613.2:p.His306ProfsTer?
ENST00000467291.5:c.916dup ENSP00000418328.1:p.His306ProfsTer?
ENST00000483043.1:c.916dup ENSP00000417392.1:p.His306ProfsTer?
ENST00000493429.5:c.916dup ENSP00000418614.1:p.His306ProfsTer?
ENST00000619575.1:c.914dup ENSP00000481717.1:p.Arg306ThrfsTer?
ENST00000622116.4:c.-507dup ENSP00000481520.1:n.-507dup
NM_001091.3:c.916dup NP_001082.2:p.His306ProfsTer?
NM_001272072.1:c.916dup NP_001259001.1:p.His306ProfsTer?
XM_011516008.1:c.916dup XP_011514310.1:p.His306ProfsTer?
XM_011516009.1:c.916dup XP_011514311.1:p.His306ProfsTer?
XR_928169.1:n.296-15938dup
XR_928170.1:n.425+11233dup
XR_928171.1:n.298-15938dup
XM_017011944.1:c.916dup XP_016867433.1:p.His306ProfsTer?
XM_017011945.1:c.916dup XP_016867434.1:p.His306ProfsTer?
XM_017011946.2:c.916dup XP_016867435.1:p.His306ProfsTer?
XM_017011947.1:c.916dup XP_016867436.1:p.His306ProfsTer?
XR_928169.2:n.302-15938dup
XR_928171.2:n.302-15938dup
NM_001091.4:c.916dup MANE Select NP_001082.2:p.His306ProfsTer?
NM_001272072.2:c.916dup NP_001259001.1:p.His306ProfsTer?