Canonical Allele Identifier: CA2685598574
Gene: AOC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150856314_150856315insTGCATAGTCCCCAGCGCCGTCGGGCCGCA , CM000669.2:g.150856314_150856315insTGCATAGTCCCCAGCGCCGTCGGGCCGCA GRCh38
NC_000007.13:g.150553402_150553403insTGCATAGTCCCCAGCGCCGTCGGGCCGCA , CM000669.1:g.150553402_150553403insTGCATAGTCCCCAGCGCCGTCGGGCCGCA GRCh37
NC_000007.12:g.150184335_150184336insTGCATAGTCCCCAGCGCCGTCGGGCCGCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA MANE Select ENSP00000354193.4:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000360937.8:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000354193.4:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000416793.6:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000411613.2:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000460213.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000418557.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000467291.5:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000418328.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000483043.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000417392.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000493429.5:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000418614.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000619575.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000481717.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGG...
ENST00000622116.4:c.-1438-141_-1438-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA ENSP00000481520.1:n.-1438-141_-1438-140insTGCATAGTCCCCAGCGCCG...
NM_001091.3:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA NP_001082.2:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA...
NM_001272072.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA NP_001259001.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...
XM_011516008.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA XP_011514310.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...
XM_011516009.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA XP_011514311.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...
XR_928169.1:n.296-14868_296-14867insCGGCCCGACGGCGCTGGGGACTATGCATG
XR_928170.1:n.425+12303_425+12304insCGGCCCGACGGCGCTGGGGACTATGCATG
XR_928171.1:n.298-14868_298-14867insCGGCCCGACGGCGCTGGGGACTATGCATG
XM_017011944.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA XP_016867433.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...
XM_017011945.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA XP_016867434.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...
XM_017011946.2:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA XP_016867435.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...
XM_017011947.1:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA XP_016867436.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...
XR_928169.2:n.302-14868_302-14867insCGGCCCGACGGCGCTGGGGACTATGCATG
XR_928171.2:n.302-14868_302-14867insCGGCCCGACGGCGCTGGGGACTATGCATG
NM_001091.4:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA MANE Select NP_001082.2:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA...
NM_001272072.2:c.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCCGCA NP_001259001.1:n.-16-141_-16-140insTGCATAGTCCCCAGCGCCGTCGGGCC...