Canonical Allele Identifier: CA2975331741
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61829674dup , CM000673.2:g.61829674dup GRCh38
NC_000011.9:g.61597146dup , CM000673.1:g.61597146dup GRCh37
NC_000011.8:g.61353722dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.207+1077dup MANE Select ENSP00000278840.4:n.207+1077dup
ENST00000257261.10:c.142-8104dup ENSP00000257261.6:n.142-8104dup
ENST00000278840.8:c.207+1077dup ENSP00000278840.4:n.207+1077dup
ENST00000517312.5:c.-160+1077dup ENSP00000430225.1:n.-160+1077dup
ENST00000518606.5:c.-160+2243dup ENSP00000430054.1:n.-160+2243dup
ENST00000521849.5:c.207+1077dup ENSP00000431091.1:n.207+1077dup
ENST00000522056.5:c.115-8104dup ENSP00000429500.1:n.115-8104dup
NM_001281501.1:c.142-8104dup NP_001268430.1:n.142-8104dup
NM_001281502.1:c.115-8104dup NP_001268431.1:n.115-8104dup
NM_004265.3:c.207+1077dup NP_004256.1:n.207+1077dup
XM_011545395.1:c.207+1077dup XP_011543697.1:n.207+1077dup
NM_004265.4:c.207+1077dup MANE Select NP_004256.1:n.207+1077dup