Canonical Allele Identifier: CA2685597947
Gene: AOC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861354_150861387del , CM000669.2:g.150861354_150861387del GRCh38
NC_000007.13:g.150558442_150558475del , CM000669.1:g.150558442_150558475del GRCh37
NC_000007.12:g.150189375_150189408del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.*145_*178del MANE Select ENSP00000354193.4:n.*145_*178del
ENST00000360937.8:c.*145_*178del ENSP00000354193.4:n.*145_*178del
ENST00000467291.5:c.*145_*178del ENSP00000418328.1:n.*145_*178del
ENST00000493429.5:c.*145_*178del ENSP00000418614.1:n.*145_*178del
XR_928169.1:n.295+15628_295+15661del
XR_928170.1:n.425+7235_425+7268del
XR_928171.1:n.297+15628_297+15661del
XR_928169.2:n.301+15628_301+15661del
XR_928171.2:n.301+15628_301+15661del
NM_001091.4:c.*145_*178del MANE Select NP_001082.2:n.*145_*178del
NM_001272072.2:c.*145_*178del NP_001259001.1:n.*145_*178del