Canonical Allele Identifier: CA1977477257

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61835005_61835007delinsCTG , CM000673.2:g.61835005_61835007delinsCTG	GRCh38
NC_000011.9:g.61602477_61602479delinsCTG , CM000673.1:g.61602477_61602479delinsCTG	GRCh37
NC_000011.8:g.61359053_61359055delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.208-2773_208-2771delinsCTG MANE Select	ENSP00000278840.4:n.208-2773_208-2771delinsCTG
ENST00000257261.10:c.142-2773_142-2771delinsCTG	ENSP00000257261.6:n.142-2773_142-2771delinsCTG
ENST00000278840.8:c.208-2773_208-2771delinsCTG	ENSP00000278840.4:n.208-2773_208-2771delinsCTG
ENST00000517312.5:c.-159-2773_-159-2771delinsCTG	ENSP00000430225.1:n.-159-2773_-159-2771delinsCTG
ENST00000518606.5:c.-159-2773_-159-2771delinsCTG	ENSP00000430054.1:n.-159-2773_-159-2771delinsCTG
ENST00000521849.5:c.208-2773_208-2771delinsCTG	ENSP00000431091.1:n.208-2773_208-2771delinsCTG
ENST00000522056.5:c.115-2773_115-2771delinsCTG	ENSP00000429500.1:n.115-2773_115-2771delinsCTG
NM_001281501.1:c.142-2773_142-2771delinsCTG	NP_001268430.1:n.142-2773_142-2771delinsCTG
NM_001281502.1:c.115-2773_115-2771delinsCTG	NP_001268431.1:n.115-2773_115-2771delinsCTG
NM_004265.3:c.208-2773_208-2771delinsCTG	NP_004256.1:n.208-2773_208-2771delinsCTG
XM_011545395.1:c.208-2773_208-2771delinsCTG	XP_011543697.1:n.208-2773_208-2771delinsCTG
NM_004265.4:c.208-2773_208-2771delinsCTG MANE Select	NP_004256.1:n.208-2773_208-2771delinsCTG