Canonical Allele Identifier: CA599518283
Gene: FADS3 HGNC NCBI

Linked Data

dbSNP Id: rs1452736409

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61887688_61887690del , CM000673.2:g.61887688_61887690del GRCh38
NC_000011.9:g.61655160_61655162del , CM000673.1:g.61655160_61655162del GRCh37
NC_000011.8:g.61411736_61411738del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278829.7:c.213+3481_213+3483del MANE Select ENSP00000278829.2:n.213+3481_213+3483del
ENST00000278829.6:c.213+3481_213+3483del ENSP00000278829.2:n.213+3481_213+3483del
ENST00000414624.6:n.286+3481_286+3483del
ENST00000525588.5:c.213+3481_213+3483del ENSP00000432206.1:n.213+3481_213+3483del
ENST00000527697.5:c.-160+4171_-160+4173del ENSP00000431533.1:n.-160+4171_-160+4173del
NM_021727.4:c.213+3481_213+3483del NP_068373.1:n.213+3481_213+3483del
XM_011545023.1:c.213+3481_213+3483del XP_011543325.1:n.213+3481_213+3483del
XM_011545023.2:c.213+3481_213+3483del XP_011543325.1:n.213+3481_213+3483del
XM_017017723.1:c.351+4171_351+4173del XP_016873212.1:n.351+4171_351+4173del
XM_017017724.1:c.351+4171_351+4173del XP_016873213.1:n.351+4171_351+4173del
XR_001747866.1:n.366+4171_366+4173del
XR_001747867.1:n.366+4171_366+4173del
XR_001747868.1:n.377+3481_377+3483del
XR_001747869.1:n.377+3481_377+3483del
NM_021727.5:c.213+3481_213+3483del MANE Select NP_068373.1:n.213+3481_213+3483del