Canonical Allele Identifier: CA1752397075
Gene: AOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150857999_150858003delinsACACT , CM000669.2:g.150857999_150858003delinsACACT GRCh38
NC_000007.13:g.150555087_150555091delinsACACT , CM000669.1:g.150555087_150555091delinsACACT GRCh37
NC_000007.12:g.150186020_150186024delinsACACT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.1529_1533delinsACACT MANE Select ENSP00000354193.4:p.His510=
ENST00000360937.8:c.1529_1533delinsACACT ENSP00000354193.4:p.His510=
ENST00000416793.6:c.1529_1533delinsACACT ENSP00000411613.2:p.His510=
ENST00000467291.5:c.1529_1533delinsACACT ENSP00000418328.1:p.His510=
ENST00000480582.1:n.67_71delinsACACT
ENST00000493429.5:c.1529_1533delinsACACT ENSP00000418614.1:p.His510=
ENST00000619575.1:c.1524_1528delinsACACT ENSP00000481717.1:p.Thr508=
ENST00000622116.4:c.107_111delinsACACT ENSP00000481520.1:p.His36=
NM_001091.3:c.1529_1533delinsACACT NP_001082.2:p.His510=
NM_001272072.1:c.1529_1533delinsACACT NP_001259001.1:p.His510=
XM_011516008.1:c.1529_1533delinsACACT XP_011514310.1:p.His510=
XM_011516009.1:c.1529_1533delinsACACT XP_011514311.1:p.His510=
XR_928169.1:n.296-16558_296-16554delinsAGTGT
XR_928170.1:n.425+10613_425+10617delinsAGTGT
XR_928171.1:n.298-16558_298-16554delinsAGTGT
XM_017011944.1:c.1529_1533delinsACACT XP_016867433.1:p.His510=
XM_017011945.1:c.1529_1533delinsACACT XP_016867434.1:p.His510=
XM_017011946.2:c.1529_1533delinsACACT XP_016867435.1:p.His510=
XM_017011947.1:c.1529_1533delinsACACT XP_016867436.1:p.His510=
XR_928169.2:n.302-16558_302-16554delinsAGTGT
XR_928171.2:n.302-16558_302-16554delinsAGTGT
NM_001091.4:c.1529_1533delinsACACT MANE Select NP_001082.2:p.His510=
NM_001272072.2:c.1529_1533delinsACACT NP_001259001.1:p.His510=