Canonical Allele Identifier: CA1977511616
Gene: FADS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61874217_61874218delinsGC , CM000673.2:g.61874217_61874218delinsGC GRCh38
NC_000011.9:g.61641689_61641690delinsGC , CM000673.1:g.61641689_61641690delinsGC GRCh37
NC_000011.8:g.61398265_61398266delinsGC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278829.7:c.1287-353_1287-352delinsGC MANE Select ENSP00000278829.2:n.1287-353_1287-352delinsGC
ENST00000278829.6:c.1287-353_1287-352delinsGC ENSP00000278829.2:n.1287-353_1287-352delinsGC
ENST00000525094.5:c.298-353_298-352delinsGC
ENST00000525588.5:c.1203-353_1203-352delinsGC ENSP00000432206.1:n.1203-353_1203-352delinsGC
ENST00000527379.5:c.638-353_638-352delinsGC
ENST00000527697.5:c.942-353_942-352delinsGC ENSP00000431533.1:n.942-353_942-352delinsGC
ENST00000529404.5:n.2041-353_2041-352delinsGC
ENST00000533676.5:n.4973-353_4973-352delinsGC
NM_021727.4:c.1287-353_1287-352delinsGC NP_068373.1:n.1287-353_1287-352delinsGC
XM_011545023.1:c.1314-353_1314-352delinsGC XP_011543325.1:n.1314-353_1314-352delinsGC
XM_011545023.2:c.1314-353_1314-352delinsGC XP_011543325.1:n.1314-353_1314-352delinsGC
XM_017017723.1:c.1452-353_1452-352delinsGC XP_016873212.1:n.1452-353_1452-352delinsGC
XM_017017724.1:c.1425-353_1425-352delinsGC XP_016873213.1:n.1425-353_1425-352delinsGC
XR_001747866.1:n.1950-353_1950-352delinsGC
XR_001747868.1:n.1961-353_1961-352delinsGC
NM_021727.5:c.1287-353_1287-352delinsGC MANE Select NP_068373.1:n.1287-353_1287-352delinsGC