Canonical Allele Identifier: CA2724190851

Gene: FADS2

Linked Data

• dbSNP Id: rs2135957709

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61835101_61835102del , CM000673.2:g.61835101_61835102del	GRCh38
NC_000011.9:g.61602573_61602574del , CM000673.1:g.61602573_61602574del	GRCh37
NC_000011.8:g.61359149_61359150del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.208-2677_208-2676del MANE Select	ENSP00000278840.4:n.208-2677_208-2676del
ENST00000257261.10:c.142-2677_142-2676del	ENSP00000257261.6:n.142-2677_142-2676del
ENST00000278840.8:c.208-2677_208-2676del	ENSP00000278840.4:n.208-2677_208-2676del
ENST00000517312.5:c.-159-2677_-159-2676del	ENSP00000430225.1:n.-159-2677_-159-2676del
ENST00000518606.5:c.-159-2677_-159-2676del	ENSP00000430054.1:n.-159-2677_-159-2676del
ENST00000521849.5:c.208-2677_208-2676del	ENSP00000431091.1:n.208-2677_208-2676del
ENST00000522056.5:c.115-2677_115-2676del	ENSP00000429500.1:n.115-2677_115-2676del
NM_001281501.1:c.142-2677_142-2676del	NP_001268430.1:n.142-2677_142-2676del
NM_001281502.1:c.115-2677_115-2676del	NP_001268431.1:n.115-2677_115-2676del
NM_004265.3:c.208-2677_208-2676del	NP_004256.1:n.208-2677_208-2676del
XM_011545395.1:c.208-2677_208-2676del	XP_011543697.1:n.208-2677_208-2676del
NM_004265.4:c.208-2677_208-2676del MANE Select	NP_004256.1:n.208-2677_208-2676del