Canonical Allele Identifier: CA679007474

Gene: FADS3

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61874245T>A , CM000673.2:g.61874245T>A	GRCh38
NC_000011.9:g.61641717T>A , CM000673.1:g.61641717T>A	GRCh37
NC_000011.8:g.61398293T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278829.7:c.1287-380A>T MANE Select	ENSP00000278829.2:n.1287-380A>T
ENST00000278829.6:c.1287-380A>T	ENSP00000278829.2:n.1287-380A>T
ENST00000525094.5:c.298-380A>T
ENST00000525588.5:c.1203-380A>T	ENSP00000432206.1:n.1203-380A>T
ENST00000527379.5:c.638-380A>T
ENST00000527697.5:c.942-380A>T	ENSP00000431533.1:n.942-380A>T
ENST00000529404.5:n.2041-380A>T
ENST00000533676.5:n.4973-380A>T
NM_021727.4:c.1287-380A>T	NP_068373.1:n.1287-380A>T
XM_011545023.1:c.1314-380A>T	XP_011543325.1:n.1314-380A>T
XM_011545023.2:c.1314-380A>T	XP_011543325.1:n.1314-380A>T
XM_017017723.1:c.1452-380A>T	XP_016873212.1:n.1452-380A>T
XM_017017724.1:c.1425-380A>T	XP_016873213.1:n.1425-380A>T
XR_001747866.1:n.1950-380A>T
XR_001747868.1:n.1961-380A>T
NM_021727.5:c.1287-380A>T MANE Select	NP_068373.1:n.1287-380A>T