Canonical Allele Identifier: CA1977474991

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61829770_61829771delinsGC , CM000673.2:g.61829770_61829771delinsGC	GRCh38
NC_000011.9:g.61597242_61597243delinsGC , CM000673.1:g.61597242_61597243delinsGC	GRCh37
NC_000011.8:g.61353818_61353819delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000278840.9:c.207+1173_207+1174delinsGC MANE Select	ENSP00000278840.4:n.207+1173_207+1174deli...
ENST00000257261.10:c.142-8008_142-8007delinsGC	ENSP00000257261.6:n.142-8008_142-8007deli...
ENST00000278840.8:c.207+1173_207+1174delinsGC	ENSP00000278840.4:n.207+1173_207+1174deli...
ENST00000517312.5:c.-160+1173_-160+1174delinsGC	ENSP00000430225.1:n.-160+1173_-160+1174de...
ENST00000518606.5:c.-160+2339_-160+2340delinsGC	ENSP00000430054.1:n.-160+2339_-160+2340de...
ENST00000521849.5:c.207+1173_207+1174delinsGC	ENSP00000431091.1:n.207+1173_207+1174deli...
ENST00000522056.5:c.115-8008_115-8007delinsGC	ENSP00000429500.1:n.115-8008_115-8007deli...
NM_001281501.1:c.142-8008_142-8007delinsGC	NP_001268430.1:n.142-8008_142-8007delinsG...
NM_001281502.1:c.115-8008_115-8007delinsGC	NP_001268431.1:n.115-8008_115-8007delinsG...
NM_004265.3:c.207+1173_207+1174delinsGC	NP_004256.1:n.207+1173_207+1174delinsGC
XM_011545395.1:c.207+1173_207+1174delinsGC	XP_011543697.1:n.207+1173_207+1174delinsG...
NM_004265.4:c.207+1173_207+1174delinsGC MANE Select	NP_004256.1:n.207+1173_207+1174delinsGC