Canonical Allele Identifier: CA403712783

Gene: ANGPTL4 ELAVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8364410C>A , CM000681.2:g.8364410C>A	GRCh38
NC_000019.9:g.8429294C>A , CM000681.1:g.8429294C>A	GRCh37
NC_000019.8:g.8335294C>A	NCBI36
NG_012169.1:g.5284C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301455.7:c.89C>A (ANGPTL4) MANE Select	ENSP00000301455.1:p.Ser30Tyr
ENST00000301455.6:c.89C>A (ANGPTL4)	ENSP00000301455.1:p.Ser30Tyr
ENST00000351593.9:c.-88+80596G>T (ELAVL1)	ENSP00000264073.6:n.-88+80596G>T
ENST00000393962.6:c.89C>A (ANGPTL4)	ENSP00000377534.1:p.Ser30Tyr
ENST00000593998.5:c.89C>A (ANGPTL4)	ENSP00000472551.1:p.Ser30Tyr
ENST00000594348.1:n.242C>A (ANGPTL4)
ENST00000594875.1:c.13C>A (ANGPTL4)
ENST00000595079.5:c.89C>A (ANGPTL4)	ENSP00000473025.1:p.Ser30Tyr
ENST00000597137.5:n.64+1048C>A (ANGPTL4)
ENST00000598255.5:n.245C>A (ANGPTL4)
ENST00000599192.5:c.89C>A (ANGPTL4)	ENSP00000473090.1:p.Ser30Tyr
ENST00000601770.1:c.89C>A (ANGPTL4)	ENSP00000471345.1:p.Ser30Tyr
ENST00000601886.1:c.89C>A (ANGPTL4)	ENSP00000470307.1:p.Ser30Tyr
NM_001039667.2:c.89C>A (ANGPTL4)	NP_001034756.1:p.Ser30Tyr
NM_139314.2:c.89C>A (ANGPTL4)	NP_647475.1:p.Ser30Tyr
NR_104213.1:n.284C>A (ANGPTL4)
XM_005272484.2:c.89C>A (ANGPTL4)	XP_005272541.1:p.Ser30Tyr
XM_005272485.2:c.89C>A (ANGPTL4)	XP_005272542.1:p.Ser30Tyr
XM_005272484.3:c.89C>A (ANGPTL4)	XP_005272541.1:p.Ser30Tyr
XM_005272485.3:c.89C>A (ANGPTL4)	XP_005272542.1:p.Ser30Tyr
NM_139314.3:c.89C>A (ANGPTL4) MANE Select	NP_647475.1:p.Ser30Tyr
NM_001039667.3:c.89C>A (ANGPTL4)	NP_001034756.1:p.Ser30Tyr
NR_104213.2:n.256C>A (ANGPTL4)