Canonical Allele Identifier: CA233370
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs66698963

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61835065_61835086del , CM000673.2:g.61835065_61835086del GRCh38
NC_000011.9:g.61602537_61602558del , CM000673.1:g.61602537_61602558del GRCh37
NC_000011.8:g.61359113_61359134del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.208-2713_208-2692del MANE Select ENSP00000278840.4:n.208-2713_208-2692del
ENST00000257261.10:c.142-2713_142-2692del ENSP00000257261.6:n.142-2713_142-2692del
ENST00000278840.8:c.208-2713_208-2692del ENSP00000278840.4:n.208-2713_208-2692del
ENST00000517312.5:c.-159-2713_-159-2692del ENSP00000430225.1:n.-159-2713_-159-2692de...
ENST00000518606.5:c.-159-2713_-159-2692del ENSP00000430054.1:n.-159-2713_-159-2692de...
ENST00000521849.5:c.208-2713_208-2692del ENSP00000431091.1:n.208-2713_208-2692del
ENST00000522056.5:c.115-2713_115-2692del ENSP00000429500.1:n.115-2713_115-2692del
NM_001281501.1:c.142-2713_142-2692del NP_001268430.1:n.142-2713_142-2692del
NM_001281502.1:c.115-2713_115-2692del NP_001268431.1:n.115-2713_115-2692del
NM_004265.3:c.208-2713_208-2692del NP_004256.1:n.208-2713_208-2692del
XM_011545395.1:c.208-2713_208-2692del XP_011543697.1:n.208-2713_208-2692del
NM_004265.4:c.208-2713_208-2692del MANE Select NP_004256.1:n.208-2713_208-2692del