Canonical Allele Identifier: CA2321386902
Gene: ANGPTL4 HGNC NCBI
ELAVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8371181G= , CM000681.2:g.8371181G= GRCh38
NC_000019.9:g.8436065G= , CM000681.1:g.8436065G= GRCh37
NC_000019.8:g.8342065G= NCBI36
NG_012169.1:g.12055G=

Transcript Alleles

HGVS Amino-acid change
ENST00000301455.7:c.757+30G= (ANGPTL4) MANE Select ENSP00000301455.1:n.757+30G=
ENST00000301455.6:c.757+30G= (ANGPTL4) ENSP00000301455.1:n.757+30G=
ENST00000351593.9:c.-88+73825C= (ELAVL1) ENSP00000264073.6:n.-88+73825C=
ENST00000393962.6:c.643+30G= (ANGPTL4) ENSP00000377534.1:n.643+30G=
ENST00000593998.5:c.757+30G= (ANGPTL4) ENSP00000472551.1:n.757+30G=
ENST00000594348.1:n.940G= (ANGPTL4)
ENST00000594875.1:c.354-3012G= (ANGPTL4)
ENST00000595079.5:c.*300+30G= (ANGPTL4) ENSP00000473025.1:n.*300+30G=
ENST00000597137.5:n.533G= (ANGPTL4)
ENST00000598255.5:n.829G= (ANGPTL4)
NM_001039667.2:c.643+30G= (ANGPTL4) NP_001034756.1:n.643+30G=
NM_139314.2:c.757+30G= (ANGPTL4) NP_647475.1:n.757+30G=
NR_104213.1:n.625-3012G= (ANGPTL4)
XM_005272484.2:c.757+30G= (ANGPTL4) XP_005272541.1:n.757+30G=
XM_005272485.2:c.643+30G= (ANGPTL4) XP_005272542.1:n.643+30G=
XM_005272484.3:c.757+30G= (ANGPTL4) XP_005272541.1:n.757+30G=
XM_005272485.3:c.643+30G= (ANGPTL4) XP_005272542.1:n.643+30G=
NM_139314.3:c.757+30G= (ANGPTL4) MANE Select NP_647475.1:n.757+30G=
NM_001039667.3:c.643+30G= (ANGPTL4) NP_001034756.1:n.643+30G=
NR_104213.2:n.597-3012G= (ANGPTL4)