Canonical Allele Identifier: CA1977474889

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61829570_61829572delinsGGT , CM000673.2:g.61829570_61829572delinsGGT	GRCh38
NC_000011.9:g.61597042_61597044delinsGGT , CM000673.1:g.61597042_61597044delinsGGT	GRCh37
NC_000011.8:g.61353618_61353620delinsGGT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000278840.9:c.207+973_207+975delinsGGT MANE Select	ENSP00000278840.4:n.207+973_207+975delins...
ENST00000257261.10:c.142-8208_142-8206delinsGGT	ENSP00000257261.6:n.142-8208_142-8206deli...
ENST00000278840.8:c.207+973_207+975delinsGGT	ENSP00000278840.4:n.207+973_207+975delins...
ENST00000517312.5:c.-160+973_-160+975delinsGGT	ENSP00000430225.1:n.-160+973_-160+975deli...
ENST00000518606.5:c.-160+2139_-160+2141delinsGGT	ENSP00000430054.1:n.-160+2139_-160+2141de...
ENST00000521849.5:c.207+973_207+975delinsGGT	ENSP00000431091.1:n.207+973_207+975delins...
ENST00000522056.5:c.115-8208_115-8206delinsGGT	ENSP00000429500.1:n.115-8208_115-8206deli...
NM_001281501.1:c.142-8208_142-8206delinsGGT	NP_001268430.1:n.142-8208_142-8206delinsG...
NM_001281502.1:c.115-8208_115-8206delinsGGT	NP_001268431.1:n.115-8208_115-8206delinsG...
NM_004265.3:c.207+973_207+975delinsGGT	NP_004256.1:n.207+973_207+975delinsGGT
XM_011545395.1:c.207+973_207+975delinsGGT	XP_011543697.1:n.207+973_207+975delinsGGT...
NM_004265.4:c.207+973_207+975delinsGGT MANE Select	NP_004256.1:n.207+973_207+975delinsGGT