Canonical Allele Identifier: CA1977511606
Gene: FADS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61874204G= , CM000673.2:g.61874204G= GRCh38
NC_000011.9:g.61641676G= , CM000673.1:g.61641676G= GRCh37
NC_000011.8:g.61398252G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278829.7:c.1287-339C= MANE Select ENSP00000278829.2:n.1287-339C=
ENST00000278829.6:c.1287-339C= ENSP00000278829.2:n.1287-339C=
ENST00000525094.5:c.298-339C=
ENST00000525588.5:c.1203-339C= ENSP00000432206.1:n.1203-339C=
ENST00000527379.5:c.638-339C=
ENST00000527697.5:c.942-339C= ENSP00000431533.1:n.942-339C=
ENST00000529404.5:n.2041-339C=
ENST00000533676.5:n.4973-339C=
NM_021727.4:c.1287-339C= NP_068373.1:n.1287-339C=
XM_011545023.1:c.1314-339C= XP_011543325.1:n.1314-339C=
XM_011545023.2:c.1314-339C= XP_011543325.1:n.1314-339C=
XM_017017723.1:c.1452-339C= XP_016873212.1:n.1452-339C=
XM_017017724.1:c.1425-339C= XP_016873213.1:n.1425-339C=
XR_001747866.1:n.1950-339C=
XR_001747868.1:n.1961-339C=
NM_021727.5:c.1287-339C= MANE Select NP_068373.1:n.1287-339C=