Canonical Allele Identifier: CA2544804753
Gene: FADS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61835062_61835073del , CM000673.2:g.61835062_61835073del GRCh38
NC_000011.9:g.61602534_61602545del , CM000673.1:g.61602534_61602545del GRCh37
NC_000011.8:g.61359110_61359121del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.208-2716_208-2705del MANE Select ENSP00000278840.4:n.208-2716_208-2705del
ENST00000257261.10:c.142-2716_142-2705del ENSP00000257261.6:n.142-2716_142-2705del
ENST00000278840.8:c.208-2716_208-2705del ENSP00000278840.4:n.208-2716_208-2705del
ENST00000517312.5:c.-159-2716_-159-2705del ENSP00000430225.1:n.-159-2716_-159-2705de...
ENST00000518606.5:c.-159-2716_-159-2705del ENSP00000430054.1:n.-159-2716_-159-2705de...
ENST00000521849.5:c.208-2716_208-2705del ENSP00000431091.1:n.208-2716_208-2705del
ENST00000522056.5:c.115-2716_115-2705del ENSP00000429500.1:n.115-2716_115-2705del
NM_001281501.1:c.142-2716_142-2705del NP_001268430.1:n.142-2716_142-2705del
NM_001281502.1:c.115-2716_115-2705del NP_001268431.1:n.115-2716_115-2705del
NM_004265.3:c.208-2716_208-2705del NP_004256.1:n.208-2716_208-2705del
XM_011545395.1:c.208-2716_208-2705del XP_011543697.1:n.208-2716_208-2705del
NM_004265.4:c.208-2716_208-2705del MANE Select NP_004256.1:n.208-2716_208-2705del