Canonical Allele Identifier: CA679007362

Gene: FADS3

Linked Data

• dbSNP Id: rs1167861142
• gnomAD v3: 11-61874062-AGACCGGGGTGACGGGTGT-A
• gnomAD v4: 11-61874062-AGACCGGGGTGACGGGTGT-A
• MyVariant Identifiers: chr11:g.61641535_61641552del (hg19) ; chr11:g.61874063_61874080del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61874063_61874080del , CM000673.2:g.61874063_61874080del	GRCh38
NC_000011.9:g.61641535_61641552del , CM000673.1:g.61641535_61641552del	GRCh37
NC_000011.8:g.61398111_61398128del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278829.7:c.1287-215_1287-198del MANE Select	ENSP00000278829.2:n.1287-215_1287-198del
ENST00000278829.6:c.1287-215_1287-198del	ENSP00000278829.2:n.1287-215_1287-198del
ENST00000525094.5:c.298-215_298-198del
ENST00000525588.5:c.1203-215_1203-198del	ENSP00000432206.1:n.1203-215_1203-198del
ENST00000527379.5:c.638-215_638-198del
ENST00000527697.5:c.942-215_942-198del	ENSP00000431533.1:n.942-215_942-198del
ENST00000529404.5:n.2041-215_2041-198del
ENST00000533676.5:n.4973-215_4973-198del
NM_021727.4:c.1287-215_1287-198del	NP_068373.1:n.1287-215_1287-198del
XM_011545023.1:c.1314-215_1314-198del	XP_011543325.1:n.1314-215_1314-198del
XM_011545023.2:c.1314-215_1314-198del	XP_011543325.1:n.1314-215_1314-198del
XM_017017723.1:c.1452-215_1452-198del	XP_016873212.1:n.1452-215_1452-198del
XM_017017724.1:c.1425-215_1425-198del	XP_016873213.1:n.1425-215_1425-198del
XR_001747866.1:n.1950-215_1950-198del
XR_001747868.1:n.1961-215_1961-198del
NM_021727.5:c.1287-215_1287-198del MANE Select	NP_068373.1:n.1287-215_1287-198del