Canonical Allele Identifier: CA2597688813

Gene: FADS3

Linked Data

• dbSNP Id: rs2136001573
• gnomAD v3: 11-61887499-GCCA-G
• gnomAD v4: 11-61887499-GCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61887500_61887502del , CM000673.2:g.61887500_61887502del	GRCh38
NC_000011.9:g.61654972_61654974del , CM000673.1:g.61654972_61654974del	GRCh37
NC_000011.8:g.61411548_61411550del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278829.7:c.213+3667_213+3669del MANE Select	ENSP00000278829.2:n.213+3667_213+3669del
ENST00000278829.6:c.213+3667_213+3669del	ENSP00000278829.2:n.213+3667_213+3669del
ENST00000414624.6:n.286+3667_286+3669del
ENST00000525588.5:c.213+3667_213+3669del	ENSP00000432206.1:n.213+3667_213+3669del
ENST00000527697.5:c.-160+4357_-160+4359del	ENSP00000431533.1:n.-160+4357_-160+4359del
NM_021727.4:c.213+3667_213+3669del	NP_068373.1:n.213+3667_213+3669del
XM_011545023.1:c.213+3667_213+3669del	XP_011543325.1:n.213+3667_213+3669del
XM_011545023.2:c.213+3667_213+3669del	XP_011543325.1:n.213+3667_213+3669del
XM_017017723.1:c.351+4357_351+4359del	XP_016873212.1:n.351+4357_351+4359del
XM_017017724.1:c.351+4357_351+4359del	XP_016873213.1:n.351+4357_351+4359del
XR_001747866.1:n.366+4357_366+4359del
XR_001747867.1:n.366+4357_366+4359del
XR_001747868.1:n.377+3667_377+3669del
XR_001747869.1:n.377+3667_377+3669del
NM_021727.5:c.213+3667_213+3669del MANE Select	NP_068373.1:n.213+3667_213+3669del