Canonical Allele Identifier: CA2792342178

Gene: FADS3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61874217G>T , CM000673.2:g.61874217G>T	GRCh38
NC_000011.9:g.61641689G>T , CM000673.1:g.61641689G>T	GRCh37
NC_000011.8:g.61398265G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000278829.7:c.1287-352C>A MANE Select	ENSP00000278829.2:n.1287-352C>A
ENST00000278829.6:c.1287-352C>A	ENSP00000278829.2:n.1287-352C>A
ENST00000525094.5:c.298-352C>A
ENST00000525588.5:c.1203-352C>A	ENSP00000432206.1:n.1203-352C>A
ENST00000527379.5:c.638-352C>A
ENST00000527697.5:c.942-352C>A	ENSP00000431533.1:n.942-352C>A
ENST00000529404.5:n.2041-352C>A
ENST00000533676.5:n.4973-352C>A
NM_021727.4:c.1287-352C>A	NP_068373.1:n.1287-352C>A
XM_011545023.1:c.1314-352C>A	XP_011543325.1:n.1314-352C>A
XM_011545023.2:c.1314-352C>A	XP_011543325.1:n.1314-352C>A
XM_017017723.1:c.1452-352C>A	XP_016873212.1:n.1452-352C>A
XM_017017724.1:c.1425-352C>A	XP_016873213.1:n.1425-352C>A
XR_001747866.1:n.1950-352C>A
XR_001747868.1:n.1961-352C>A
NM_021727.5:c.1287-352C>A MANE Select	NP_068373.1:n.1287-352C>A