Canonical Allele Identifier: CA1977488235
Gene: FADS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61887846_61887847delinsTG , CM000673.2:g.61887846_61887847delinsTG GRCh38
NC_000011.9:g.61655318_61655319delinsTG , CM000673.1:g.61655318_61655319delinsTG GRCh37
NC_000011.8:g.61411894_61411895delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278829.7:c.213+3322_213+3323delinsCA MANE Select ENSP00000278829.2:n.213+3322_213+3323delinsCA
ENST00000278829.6:c.213+3322_213+3323delinsCA ENSP00000278829.2:n.213+3322_213+3323delinsCA
ENST00000414624.6:n.286+3322_286+3323delinsCA
ENST00000525588.5:c.213+3322_213+3323delinsCA ENSP00000432206.1:n.213+3322_213+3323delinsCA
ENST00000527697.5:c.-160+4012_-160+4013delinsCA ENSP00000431533.1:n.-160+4012_-160+4013delinsCA
NM_021727.4:c.213+3322_213+3323delinsCA NP_068373.1:n.213+3322_213+3323delinsCA
XM_011545023.1:c.213+3322_213+3323delinsCA XP_011543325.1:n.213+3322_213+3323delinsCA
XM_011545023.2:c.213+3322_213+3323delinsCA XP_011543325.1:n.213+3322_213+3323delinsCA
XM_017017723.1:c.351+4012_351+4013delinsCA XP_016873212.1:n.351+4012_351+4013delinsCA
XM_017017724.1:c.351+4012_351+4013delinsCA XP_016873213.1:n.351+4012_351+4013delinsCA
XR_001747866.1:n.366+4012_366+4013delinsCA
XR_001747867.1:n.366+4012_366+4013delinsCA
XR_001747868.1:n.377+3322_377+3323delinsCA
XR_001747869.1:n.377+3322_377+3323delinsCA
NM_021727.5:c.213+3322_213+3323delinsCA MANE Select NP_068373.1:n.213+3322_213+3323delinsCA