Canonical Allele Identifier: CA1977488244

Gene: FADS3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61887862_61887863delinsAC , CM000673.2:g.61887862_61887863delinsAC	GRCh38
NC_000011.9:g.61655334_61655335delinsAC , CM000673.1:g.61655334_61655335delinsAC	GRCh37
NC_000011.8:g.61411910_61411911delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278829.7:c.213+3306_213+3307delinsGT MANE Select	ENSP00000278829.2:n.213+3306_213+3307delinsGT
ENST00000278829.6:c.213+3306_213+3307delinsGT	ENSP00000278829.2:n.213+3306_213+3307delinsGT
ENST00000414624.6:n.286+3306_286+3307delinsGT
ENST00000525588.5:c.213+3306_213+3307delinsGT	ENSP00000432206.1:n.213+3306_213+3307delinsGT
ENST00000527697.5:c.-160+3996_-160+3997delinsGT	ENSP00000431533.1:n.-160+3996_-160+3997delinsGT
NM_021727.4:c.213+3306_213+3307delinsGT	NP_068373.1:n.213+3306_213+3307delinsGT
XM_011545023.1:c.213+3306_213+3307delinsGT	XP_011543325.1:n.213+3306_213+3307delinsGT
XM_011545023.2:c.213+3306_213+3307delinsGT	XP_011543325.1:n.213+3306_213+3307delinsGT
XM_017017723.1:c.351+3996_351+3997delinsGT	XP_016873212.1:n.351+3996_351+3997delinsGT
XM_017017724.1:c.351+3996_351+3997delinsGT	XP_016873213.1:n.351+3996_351+3997delinsGT
XR_001747866.1:n.366+3996_366+3997delinsGT
XR_001747867.1:n.366+3996_366+3997delinsGT
XR_001747868.1:n.377+3306_377+3307delinsGT
XR_001747869.1:n.377+3306_377+3307delinsGT
NM_021727.5:c.213+3306_213+3307delinsGT MANE Select	NP_068373.1:n.213+3306_213+3307delinsGT