Canonical Allele Identifier: CA1977498996

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61803914C= , CM000673.2:g.61803914C= GRCh38
NC_000011.9:g.61571386C= , CM000673.1:g.61571386C= GRCh37
NC_000011.8:g.61327962C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000350997.12:c.1054-147G= (FADS1) MANE Select ENSP00000322229.9:n.1054-147G=
ENST00000350997.11:c.1054-147G= (FADS1) ENSP00000322229.9:n.1054-147G=
ENST00000433932.5:c.631-147G= (FADS1) ENSP00000405087.1:n.631-147G=
ENST00000460649.5:c.-159G= (FADS1) ENSP00000445253.1:n.-159G=
ENST00000496123.6:n.328-147G= (FADS1)
ENST00000536991.5:c.127-147G= (FADS1) ENSP00000439097.1:n.127-147G=
ENST00000539999.1:c.241-147G= (FADS1) ENSP00000443587.1:n.241-147G=
ENST00000542506.5:c.631-147G= (FADS1) ENSP00000441403.1:n.631-147G=
ENST00000574708.5:c.-55+10886C= (FADS2) ENSP00000458917.1:n.-55+10886C=
NM_013402.4:c.1054-147G= (FADS1) NP_037534.3:n.1054-147G=
XM_011545022.1:c.841-147G= (FADS1) XP_011543324.1:n.841-147G=
NM_013402.6:c.1054-147G= (FADS1) NP_037534.5:n.1054-147G=
XM_011545022.2:c.841-147G= (FADS1) XP_011543324.1:n.841-147G=
NM_013402.7:c.1054-147G= (FADS1) MANE Select NP_037534.5:n.1054-147G=