Canonical Allele Identifier: CA1752388564
Gene: AOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861347_150861363delinsAACAGACGTGCACACAC , CM000669.2:g.150861347_150861363delinsAACAGACGTGCACACAC GRCh38
NC_000007.13:g.150558435_150558451delinsAACAGACGTGCACACAC , CM000669.1:g.150558435_150558451delinsAACAGACGTGCACACAC GRCh37
NC_000007.12:g.150189368_150189384delinsAACAGACGTGCACACAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.*138_*154delinsAACAGACGTGCACACAC MANE Select ENSP00000354193.4:n.*138_*154delinsAACAGACGTGCACACAC
ENST00000360937.8:c.*138_*154delinsAACAGACGTGCACACAC ENSP00000354193.4:n.*138_*154delinsAACAGACGTGCACACAC
ENST00000467291.5:c.*138_*154delinsAACAGACGTGCACACAC ENSP00000418328.1:n.*138_*154delinsAACAGACGTGCACACAC
ENST00000493429.5:c.*138_*154delinsAACAGACGTGCACACAC ENSP00000418614.1:n.*138_*154delinsAACAGACGTGCACACAC
XR_928169.1:n.295+15646_295+15662delinsGTGTGTGCACGTCTGTT
XR_928170.1:n.425+7253_425+7269delinsGTGTGTGCACGTCTGTT
XR_928171.1:n.297+15646_297+15662delinsGTGTGTGCACGTCTGTT
XR_928169.2:n.301+15646_301+15662delinsGTGTGTGCACGTCTGTT
XR_928171.2:n.301+15646_301+15662delinsGTGTGTGCACGTCTGTT
NM_001091.4:c.*138_*154delinsAACAGACGTGCACACAC MANE Select NP_001082.2:n.*138_*154delinsAACAGACGTGCACACAC
NM_001272072.2:c.*138_*154delinsAACAGACGTGCACACAC NP_001259001.1:n.*138_*154delinsAACAGACGTGCACACAC