Canonical Allele Identifier: CA938622120
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs2067160712

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61835042_61835043del , CM000673.2:g.61835042_61835043del GRCh38
NC_000011.9:g.61602514_61602515del , CM000673.1:g.61602514_61602515del GRCh37
NC_000011.8:g.61359090_61359091del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278840.9:c.208-2736_208-2735del MANE Select ENSP00000278840.4:n.208-2736_208-2735del
ENST00000257261.10:c.142-2736_142-2735del ENSP00000257261.6:n.142-2736_142-2735del
ENST00000278840.8:c.208-2736_208-2735del ENSP00000278840.4:n.208-2736_208-2735del
ENST00000517312.5:c.-159-2736_-159-2735del ENSP00000430225.1:n.-159-2736_-159-2735del
ENST00000518606.5:c.-159-2736_-159-2735del ENSP00000430054.1:n.-159-2736_-159-2735del
ENST00000521849.5:c.208-2736_208-2735del ENSP00000431091.1:n.208-2736_208-2735del
ENST00000522056.5:c.115-2736_115-2735del ENSP00000429500.1:n.115-2736_115-2735del
NM_001281501.1:c.142-2736_142-2735del NP_001268430.1:n.142-2736_142-2735del
NM_001281502.1:c.115-2736_115-2735del NP_001268431.1:n.115-2736_115-2735del
NM_004265.3:c.208-2736_208-2735del NP_004256.1:n.208-2736_208-2735del
XM_011545395.1:c.208-2736_208-2735del XP_011543697.1:n.208-2736_208-2735del
NM_004265.4:c.208-2736_208-2735del MANE Select NP_004256.1:n.208-2736_208-2735del