Canonical Allele Identifier: CA1977511585
Gene: FADS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61874164T= , CM000673.2:g.61874164T= GRCh38
NC_000011.9:g.61641636T= , CM000673.1:g.61641636T= GRCh37
NC_000011.8:g.61398212T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278829.7:c.1287-299A= MANE Select ENSP00000278829.2:n.1287-299A=
ENST00000278829.6:c.1287-299A= ENSP00000278829.2:n.1287-299A=
ENST00000525094.5:c.298-299A=
ENST00000525588.5:c.1203-299A= ENSP00000432206.1:n.1203-299A=
ENST00000527379.5:c.638-299A=
ENST00000527697.5:c.942-299A= ENSP00000431533.1:n.942-299A=
ENST00000529404.5:n.2041-299A=
ENST00000533676.5:n.4973-299A=
NM_021727.4:c.1287-299A= NP_068373.1:n.1287-299A=
XM_011545023.1:c.1314-299A= XP_011543325.1:n.1314-299A=
XM_011545023.2:c.1314-299A= XP_011543325.1:n.1314-299A=
XM_017017723.1:c.1452-299A= XP_016873212.1:n.1452-299A=
XM_017017724.1:c.1425-299A= XP_016873213.1:n.1425-299A=
XR_001747866.1:n.1950-299A=
XR_001747868.1:n.1961-299A=
NM_021727.5:c.1287-299A= MANE Select NP_068373.1:n.1287-299A=