Canonical Allele Identifier: CA1977474626

Gene: FADS2 FADS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61828986G= , CM000673.2:g.61828986G=	GRCh38
NC_000011.9:g.61596458G= , CM000673.1:g.61596458G=	GRCh37
NC_000011.8:g.61353034G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000278840.9:c.207+389G= (FADS2) MANE Select	ENSP00000278840.4:n.207+389G=
ENST00000257261.10:c.142-8792G= (FADS2)	ENSP00000257261.6:n.142-8792G=
ENST00000278840.8:c.207+389G= (FADS2)	ENSP00000278840.4:n.207+389G=
ENST00000421879.5:c.-49+215C= (FADS1)	ENSP00000416043.1:n.-49+215C=
ENST00000448607.1:c.-308+215C= (FADS1)	ENSP00000391229.1:n.-308+215C=
ENST00000517312.5:c.-160+389G= (FADS2)	ENSP00000430225.1:n.-160+389G=
ENST00000518606.5:c.-160+1555G= (FADS2)	ENSP00000430054.1:n.-160+1555G=
ENST00000521849.5:c.207+389G= (FADS2)	ENSP00000431091.1:n.207+389G=
ENST00000522056.5:c.115-8792G= (FADS2)	ENSP00000429500.1:n.115-8792G=
NM_001281501.1:c.142-8792G= (FADS2)	NP_001268430.1:n.142-8792G=
NM_001281502.1:c.115-8792G= (FADS2)	NP_001268431.1:n.115-8792G=
NM_004265.3:c.207+389G= (FADS2)	NP_004256.1:n.207+389G=
XM_011545395.1:c.207+389G= (FADS2)	XP_011543697.1:n.207+389G=
NM_004265.4:c.207+389G= (FADS2) MANE Select	NP_004256.1:n.207+389G=