Canonical Allele Identifier: CA2975332068

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61830446_61830447insG , CM000673.2:g.61830446_61830447insG	GRCh38
NC_000011.9:g.61597918_61597919insG , CM000673.1:g.61597918_61597919insG	GRCh37
NC_000011.8:g.61354494_61354495insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.207+1849_207+1850insG MANE Select	ENSP00000278840.4:n.207+1849_207+1850insG
ENST00000257261.10:c.142-7332_142-7331insG	ENSP00000257261.6:n.142-7332_142-7331insG
ENST00000278840.8:c.207+1849_207+1850insG	ENSP00000278840.4:n.207+1849_207+1850insG
ENST00000517312.5:c.-160+1849_-160+1850insG	ENSP00000430225.1:n.-160+1849_-160+1850insG
ENST00000518606.5:c.-160+3015_-160+3016insG	ENSP00000430054.1:n.-160+3015_-160+3016insG
ENST00000521849.5:c.207+1849_207+1850insG	ENSP00000431091.1:n.207+1849_207+1850insG
ENST00000522056.5:c.115-7332_115-7331insG	ENSP00000429500.1:n.115-7332_115-7331insG
NM_001281501.1:c.142-7332_142-7331insG	NP_001268430.1:n.142-7332_142-7331insG
NM_001281502.1:c.115-7332_115-7331insG	NP_001268431.1:n.115-7332_115-7331insG
NM_004265.3:c.207+1849_207+1850insG	NP_004256.1:n.207+1849_207+1850insG
XM_011545395.1:c.207+1849_207+1850insG	XP_011543697.1:n.207+1849_207+1850insG
NM_004265.4:c.207+1849_207+1850insG MANE Select	NP_004256.1:n.207+1849_207+1850insG