Canonical Allele Identifier: CA2321386904
Gene: ANGPTL4 HGNC NCBI
ELAVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8371183G= , CM000681.2:g.8371183G= GRCh38
NC_000019.9:g.8436067G= , CM000681.1:g.8436067G= GRCh37
NC_000019.8:g.8342067G= NCBI36
NG_012169.1:g.12057G=

Transcript Alleles

HGVS Amino-acid change
ENST00000301455.7:c.757+32G= (ANGPTL4) MANE Select ENSP00000301455.1:n.757+32G=
ENST00000301455.6:c.757+32G= (ANGPTL4) ENSP00000301455.1:n.757+32G=
ENST00000351593.9:c.-88+73823C= (ELAVL1) ENSP00000264073.6:n.-88+73823C=
ENST00000393962.6:c.643+32G= (ANGPTL4) ENSP00000377534.1:n.643+32G=
ENST00000593998.5:c.757+32G= (ANGPTL4) ENSP00000472551.1:n.757+32G=
ENST00000594348.1:n.942G= (ANGPTL4)
ENST00000594875.1:c.354-3010G= (ANGPTL4)
ENST00000595079.5:c.*300+32G= (ANGPTL4) ENSP00000473025.1:n.*300+32G=
ENST00000597137.5:n.535G= (ANGPTL4)
ENST00000598255.5:n.831G= (ANGPTL4)
NM_001039667.2:c.643+32G= (ANGPTL4) NP_001034756.1:n.643+32G=
NM_139314.2:c.757+32G= (ANGPTL4) NP_647475.1:n.757+32G=
NR_104213.1:n.625-3010G= (ANGPTL4)
XM_005272484.2:c.757+32G= (ANGPTL4) XP_005272541.1:n.757+32G=
XM_005272485.2:c.643+32G= (ANGPTL4) XP_005272542.1:n.643+32G=
XM_005272484.3:c.757+32G= (ANGPTL4) XP_005272541.1:n.757+32G=
XM_005272485.3:c.643+32G= (ANGPTL4) XP_005272542.1:n.643+32G=
NM_139314.3:c.757+32G= (ANGPTL4) MANE Select NP_647475.1:n.757+32G=
NM_001039667.3:c.643+32G= (ANGPTL4) NP_001034756.1:n.643+32G=
NR_104213.2:n.597-3010G= (ANGPTL4)