Canonical Allele Identifier: CA2556998770

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61835046_61835064del , CM000673.2:g.61835046_61835064del	GRCh38
NC_000011.9:g.61602518_61602536del , CM000673.1:g.61602518_61602536del	GRCh37
NC_000011.8:g.61359094_61359112del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.208-2732_208-2714del MANE Select	ENSP00000278840.4:n.208-2732_208-2714del
ENST00000257261.10:c.142-2732_142-2714del	ENSP00000257261.6:n.142-2732_142-2714del
ENST00000278840.8:c.208-2732_208-2714del	ENSP00000278840.4:n.208-2732_208-2714del
ENST00000517312.5:c.-159-2732_-159-2714del	ENSP00000430225.1:n.-159-2732_-159-2714del
ENST00000518606.5:c.-159-2732_-159-2714del	ENSP00000430054.1:n.-159-2732_-159-2714del
ENST00000521849.5:c.208-2732_208-2714del	ENSP00000431091.1:n.208-2732_208-2714del
ENST00000522056.5:c.115-2732_115-2714del	ENSP00000429500.1:n.115-2732_115-2714del
NM_001281501.1:c.142-2732_142-2714del	NP_001268430.1:n.142-2732_142-2714del
NM_001281502.1:c.115-2732_115-2714del	NP_001268431.1:n.115-2732_115-2714del
NM_004265.3:c.208-2732_208-2714del	NP_004256.1:n.208-2732_208-2714del
XM_011545395.1:c.208-2732_208-2714del	XP_011543697.1:n.208-2732_208-2714del
NM_004265.4:c.208-2732_208-2714del MANE Select	NP_004256.1:n.208-2732_208-2714del