Canonical Allele Identifier: CA1977475275

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61830410_61830413delinsCTTG , CM000673.2:g.61830410_61830413delinsCTTG	GRCh38
NC_000011.9:g.61597882_61597885delinsCTTG , CM000673.1:g.61597882_61597885delinsCTTG	GRCh37
NC_000011.8:g.61354458_61354461delinsCTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.207+1813_207+1816delinsCTTG MANE Select	ENSP00000278840.4:n.207+1813_207+1816delinsCTTG
ENST00000257261.10:c.142-7368_142-7365delinsCTTG	ENSP00000257261.6:n.142-7368_142-7365delinsCTTG
ENST00000278840.8:c.207+1813_207+1816delinsCTTG	ENSP00000278840.4:n.207+1813_207+1816delinsCTTG
ENST00000517312.5:c.-160+1813_-160+1816delinsCTTG	ENSP00000430225.1:n.-160+1813_-160+1816delinsCTTG
ENST00000518606.5:c.-160+2979_-160+2982delinsCTTG	ENSP00000430054.1:n.-160+2979_-160+2982delinsCTTG
ENST00000521849.5:c.207+1813_207+1816delinsCTTG	ENSP00000431091.1:n.207+1813_207+1816delinsCTTG
ENST00000522056.5:c.115-7368_115-7365delinsCTTG	ENSP00000429500.1:n.115-7368_115-7365delinsCTTG
NM_001281501.1:c.142-7368_142-7365delinsCTTG	NP_001268430.1:n.142-7368_142-7365delinsCTTG
NM_001281502.1:c.115-7368_115-7365delinsCTTG	NP_001268431.1:n.115-7368_115-7365delinsCTTG
NM_004265.3:c.207+1813_207+1816delinsCTTG	NP_004256.1:n.207+1813_207+1816delinsCTTG
XM_011545395.1:c.207+1813_207+1816delinsCTTG	XP_011543697.1:n.207+1813_207+1816delinsCTTG
NM_004265.4:c.207+1813_207+1816delinsCTTG MANE Select	NP_004256.1:n.207+1813_207+1816delinsCTTG