Canonical Allele Identifier: CA169071216
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs386719405

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150846598_150846599delinsTG , CM000669.2:g.150846598_150846599delinsTG GRCh38
NC_000007.13:g.150543686_150543687delinsTG , CM000669.1:g.150543686_150543687delinsTG GRCh37
NC_000007.12:g.150174619_150174620delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467291.5:c.-92-5517_-92-5516delinsTG ENSP00000418328.1:n.-92-5517_-92-5516delinsTG
ENST00000493429.5:c.-92-5517_-92-5516delinsTG ENSP00000418614.1:n.-92-5517_-92-5516delinsTG
XM_011516008.1:c.-181-5517_-181-5516delinsTG XP_011514310.1:n.-181-5517_-181-5516delinsTG
XM_011516009.1:c.-92-5517_-92-5516delinsTG XP_011514311.1:n.-92-5517_-92-5516delinsTG
XR_928169.1:n.296-5154_296-5153delinsCA
XR_928170.1:n.426-5154_426-5153delinsCA
XR_928171.1:n.298-5154_298-5153delinsCA
XM_017011944.1:c.-92-5517_-92-5516delinsTG XP_016867433.1:n.-92-5517_-92-5516delinsTG
XM_017011945.1:c.-92-5517_-92-5516delinsTG XP_016867434.1:n.-92-5517_-92-5516delinsTG
XR_928169.2:n.302-5154_302-5153delinsCA
XR_928171.2:n.302-5154_302-5153delinsCA