Canonical Allele Identifier: CA1977477210
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61834970_61835046delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT , CM000673.2:g.61834970_61835046delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT GRCh38
NC_000011.9:g.61602442_61602518delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT , CM000673.1:g.61602442_61602518delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT GRCh37
NC_000011.8:g.61359018_61359094delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.208-2808_208-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT MANE Select ENSP00000278840.4:n.208-2808_208-2732deli...
ENST00000257261.10:c.142-2808_142-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT ENSP00000257261.6:n.142-2808_142-2732deli...
ENST00000278840.8:c.208-2808_208-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT ENSP00000278840.4:n.208-2808_208-2732deli...
ENST00000517312.5:c.-159-2808_-159-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT ENSP00000430225.1:n.-159-2808_-159-2732de...
ENST00000518606.5:c.-159-2808_-159-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT ENSP00000430054.1:n.-159-2808_-159-2732de...
ENST00000521849.5:c.208-2808_208-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT ENSP00000431091.1:n.208-2808_208-2732deli...
ENST00000522056.5:c.115-2808_115-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT ENSP00000429500.1:n.115-2808_115-2732deli...
NM_001281501.1:c.142-2808_142-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT NP_001268430.1:n.142-2808_142-2732delinsC...
NM_001281502.1:c.115-2808_115-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT NP_001268431.1:n.115-2808_115-2732delinsC...
NM_004265.3:c.208-2808_208-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT NP_004256.1:n.208-2808_208-2732delinsCCTC...
XM_011545395.1:c.208-2808_208-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT XP_011543697.1:n.208-2808_208-2732delinsC...
NM_004265.4:c.208-2808_208-2732delinsCCTCCCTGCCTGCCCCCCCACCCCAGCCCTCCTCCCTGCCTGCCCCCAGGGCCTCCTCCCTGCCTCCCCAGGGACTT MANE Select NP_004256.1:n.208-2808_208-2732delinsCCTC...