Canonical Allele Identifier: CA2685598771
Gene: AOC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150856357G>T , CM000669.2:g.150856357G>T GRCh38
NC_000007.13:g.150553445G>T , CM000669.1:g.150553445G>T GRCh37
NC_000007.12:g.150184378G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360937.9:c.-16-98G>T MANE Select ENSP00000354193.4:n.-16-98G>T
ENST00000360937.8:c.-16-98G>T ENSP00000354193.4:n.-16-98G>T
ENST00000416793.6:c.-16-98G>T ENSP00000411613.2:n.-16-98G>T
ENST00000460213.1:c.-16-98G>T ENSP00000418557.1:n.-16-98G>T
ENST00000467291.5:c.-16-98G>T ENSP00000418328.1:n.-16-98G>T
ENST00000483043.1:c.-16-98G>T ENSP00000417392.1:n.-16-98G>T
ENST00000493429.5:c.-16-98G>T ENSP00000418614.1:n.-16-98G>T
ENST00000619575.1:c.-16-98G>T ENSP00000481717.1:n.-16-98G>T
ENST00000622116.4:c.-1438-98G>T ENSP00000481520.1:n.-1438-98G>T
NM_001091.3:c.-16-98G>T NP_001082.2:n.-16-98G>T
NM_001272072.1:c.-16-98G>T NP_001259001.1:n.-16-98G>T
XM_011516008.1:c.-16-98G>T XP_011514310.1:n.-16-98G>T
XM_011516009.1:c.-16-98G>T XP_011514311.1:n.-16-98G>T
XR_928169.1:n.296-14912C>A
XR_928170.1:n.425+12259C>A
XR_928171.1:n.298-14912C>A
XM_017011944.1:c.-16-98G>T XP_016867433.1:n.-16-98G>T
XM_017011945.1:c.-16-98G>T XP_016867434.1:n.-16-98G>T
XM_017011946.2:c.-16-98G>T XP_016867435.1:n.-16-98G>T
XM_017011947.1:c.-16-98G>T XP_016867436.1:n.-16-98G>T
XR_928169.2:n.302-14912C>A
XR_928171.2:n.302-14912C>A
NM_001091.4:c.-16-98G>T MANE Select NP_001082.2:n.-16-98G>T
NM_001272072.2:c.-16-98G>T NP_001259001.1:n.-16-98G>T