Canonical Allele Identifier: CA1977474974

Gene: FADS2

Linked Data

• dbSNP Id: rs2067112359

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61829716_61829730dup , CM000673.2:g.61829716_61829730dup	GRCh38
NC_000011.9:g.61597188_61597202dup , CM000673.1:g.61597188_61597202dup	GRCh37
NC_000011.8:g.61353764_61353778dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000278840.9:c.207+1119_207+1133dup MANE Select	ENSP00000278840.4:n.207+1119_207+1133dup
ENST00000257261.10:c.142-8062_142-8048dup	ENSP00000257261.6:n.142-8062_142-8048dup
ENST00000278840.8:c.207+1119_207+1133dup	ENSP00000278840.4:n.207+1119_207+1133dup
ENST00000517312.5:c.-160+1119_-160+1133dup	ENSP00000430225.1:n.-160+1119_-160+1133du...
ENST00000518606.5:c.-160+2285_-160+2299dup	ENSP00000430054.1:n.-160+2285_-160+2299du...
ENST00000521849.5:c.207+1119_207+1133dup	ENSP00000431091.1:n.207+1119_207+1133dup
ENST00000522056.5:c.115-8062_115-8048dup	ENSP00000429500.1:n.115-8062_115-8048dup
NM_001281501.1:c.142-8062_142-8048dup	NP_001268430.1:n.142-8062_142-8048dup
NM_001281502.1:c.115-8062_115-8048dup	NP_001268431.1:n.115-8062_115-8048dup
NM_004265.3:c.207+1119_207+1133dup	NP_004256.1:n.207+1119_207+1133dup
XM_011545395.1:c.207+1119_207+1133dup	XP_011543697.1:n.207+1119_207+1133dup
NM_004265.4:c.207+1119_207+1133dup MANE Select	NP_004256.1:n.207+1119_207+1133dup