Canonical Allele Identifier: CA1977488048
Gene: FADS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61887386T= , CM000673.2:g.61887386T= GRCh38
NC_000011.9:g.61654858T= , CM000673.1:g.61654858T= GRCh37
NC_000011.8:g.61411434T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278829.7:c.213+3783A= MANE Select ENSP00000278829.2:n.213+3783A=
ENST00000278829.6:c.213+3783A= ENSP00000278829.2:n.213+3783A=
ENST00000414624.6:n.286+3783A=
ENST00000525588.5:c.213+3783A= ENSP00000432206.1:n.213+3783A=
ENST00000527697.5:c.-160+4473A= ENSP00000431533.1:n.-160+4473A=
NM_021727.4:c.213+3783A= NP_068373.1:n.213+3783A=
XM_011545023.1:c.213+3783A= XP_011543325.1:n.213+3783A=
XM_011545023.2:c.213+3783A= XP_011543325.1:n.213+3783A=
XM_017017723.1:c.351+4473A= XP_016873212.1:n.351+4473A=
XM_017017724.1:c.351+4473A= XP_016873213.1:n.351+4473A=
XR_001747866.1:n.366+4473A=
XR_001747867.1:n.366+4473A=
XR_001747868.1:n.377+3783A=
XR_001747869.1:n.377+3783A=
NM_021727.5:c.213+3783A= MANE Select NP_068373.1:n.213+3783A=