Canonical Allele Identifier: CA918894304

Gene: FADS2

Linked Data

• dbSNP Id: rs1565326913

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61829491_61829498dup , CM000673.2:g.61829491_61829498dup	GRCh38
NC_000011.9:g.61596963_61596970dup , CM000673.1:g.61596963_61596970dup	GRCh37
NC_000011.8:g.61353539_61353546dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.207+894_207+901dup MANE Select	ENSP00000278840.4:n.207+894_207+901dup
ENST00000257261.10:c.142-8287_142-8280dup	ENSP00000257261.6:n.142-8287_142-8280dup
ENST00000278840.8:c.207+894_207+901dup	ENSP00000278840.4:n.207+894_207+901dup
ENST00000517312.5:c.-160+894_-160+901dup	ENSP00000430225.1:n.-160+894_-160+901dup
ENST00000518606.5:c.-160+2060_-160+2067dup	ENSP00000430054.1:n.-160+2060_-160+2067dup
ENST00000521849.5:c.207+894_207+901dup	ENSP00000431091.1:n.207+894_207+901dup
ENST00000522056.5:c.115-8287_115-8280dup	ENSP00000429500.1:n.115-8287_115-8280dup
NM_001281501.1:c.142-8287_142-8280dup	NP_001268430.1:n.142-8287_142-8280dup
NM_001281502.1:c.115-8287_115-8280dup	NP_001268431.1:n.115-8287_115-8280dup
NM_004265.3:c.207+894_207+901dup	NP_004256.1:n.207+894_207+901dup
XM_011545395.1:c.207+894_207+901dup	XP_011543697.1:n.207+894_207+901dup
NM_004265.4:c.207+894_207+901dup MANE Select	NP_004256.1:n.207+894_207+901dup