Canonical Allele Identifier: CA2792334815

Gene: FADS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61834979_61834980insAG , CM000673.2:g.61834979_61834980insAG	GRCh38
NC_000011.9:g.61602451_61602452insAG , CM000673.1:g.61602451_61602452insAG	GRCh37
NC_000011.8:g.61359027_61359028insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.208-2799_208-2798insAG MANE Select	ENSP00000278840.4:n.208-2799_208-2798insAG
ENST00000257261.10:c.142-2799_142-2798insAG	ENSP00000257261.6:n.142-2799_142-2798insAG
ENST00000278840.8:c.208-2799_208-2798insAG	ENSP00000278840.4:n.208-2799_208-2798insAG
ENST00000517312.5:c.-159-2799_-159-2798insAG	ENSP00000430225.1:n.-159-2799_-159-2798insAG
ENST00000518606.5:c.-159-2799_-159-2798insAG	ENSP00000430054.1:n.-159-2799_-159-2798insAG
ENST00000521849.5:c.208-2799_208-2798insAG	ENSP00000431091.1:n.208-2799_208-2798insAG
ENST00000522056.5:c.115-2799_115-2798insAG	ENSP00000429500.1:n.115-2799_115-2798insAG
NM_001281501.1:c.142-2799_142-2798insAG	NP_001268430.1:n.142-2799_142-2798insAG
NM_001281502.1:c.115-2799_115-2798insAG	NP_001268431.1:n.115-2799_115-2798insAG
NM_004265.3:c.208-2799_208-2798insAG	NP_004256.1:n.208-2799_208-2798insAG
XM_011545395.1:c.208-2799_208-2798insAG	XP_011543697.1:n.208-2799_208-2798insAG
NM_004265.4:c.208-2799_208-2798insAG MANE Select	NP_004256.1:n.208-2799_208-2798insAG