Canonical Allele Identifier: CA1977474916
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61829628_61829629delinsAG , CM000673.2:g.61829628_61829629delinsAG GRCh38
NC_000011.9:g.61597100_61597101delinsAG , CM000673.1:g.61597100_61597101delinsAG GRCh37
NC_000011.8:g.61353676_61353677delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.207+1031_207+1032delinsAG MANE Select ENSP00000278840.4:n.207+1031_207+1032deli...
ENST00000257261.10:c.142-8150_142-8149delinsAG ENSP00000257261.6:n.142-8150_142-8149deli...
ENST00000278840.8:c.207+1031_207+1032delinsAG ENSP00000278840.4:n.207+1031_207+1032deli...
ENST00000517312.5:c.-160+1031_-160+1032delinsAG ENSP00000430225.1:n.-160+1031_-160+1032de...
ENST00000518606.5:c.-160+2197_-160+2198delinsAG ENSP00000430054.1:n.-160+2197_-160+2198de...
ENST00000521849.5:c.207+1031_207+1032delinsAG ENSP00000431091.1:n.207+1031_207+1032deli...
ENST00000522056.5:c.115-8150_115-8149delinsAG ENSP00000429500.1:n.115-8150_115-8149deli...
NM_001281501.1:c.142-8150_142-8149delinsAG NP_001268430.1:n.142-8150_142-8149delinsA...
NM_001281502.1:c.115-8150_115-8149delinsAG NP_001268431.1:n.115-8150_115-8149delinsA...
NM_004265.3:c.207+1031_207+1032delinsAG NP_004256.1:n.207+1031_207+1032delinsAG
XM_011545395.1:c.207+1031_207+1032delinsAG XP_011543697.1:n.207+1031_207+1032delinsA...
NM_004265.4:c.207+1031_207+1032delinsAG MANE Select NP_004256.1:n.207+1031_207+1032delinsAG