Canonical Allele Identifier: CA9155861

Gene: ANGPTL4 ELAVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8364507C>T , CM000681.2:g.8364507C>T	GRCh38
NC_000019.9:g.8429391C>T , CM000681.1:g.8429391C>T	GRCh37
NC_000019.8:g.8335391C>T	NCBI36
NG_012169.1:g.5381C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301455.7:c.186C>T (ANGPTL4) MANE Select	ENSP00000301455.1:p.Thr62=
ENST00000301455.6:c.186C>T (ANGPTL4)	ENSP00000301455.1:p.Thr62=
ENST00000351593.9:c.-88+80499G>A (ELAVL1)	ENSP00000264073.6:n.-88+80499G>A
ENST00000393962.6:c.186C>T (ANGPTL4)	ENSP00000377534.1:p.Thr62=
ENST00000593998.5:c.186C>T (ANGPTL4)	ENSP00000472551.1:p.Thr62=
ENST00000594348.1:n.339C>T (ANGPTL4)
ENST00000594875.1:c.110C>T (ANGPTL4)
ENST00000595079.5:c.186C>T (ANGPTL4)	ENSP00000473025.1:p.Thr62=
ENST00000597137.5:n.64+1145C>T (ANGPTL4)
ENST00000598255.5:n.342C>T (ANGPTL4)
ENST00000599192.5:c.186C>T (ANGPTL4)	ENSP00000473090.1:p.Thr62=
ENST00000601770.1:c.186C>T (ANGPTL4)	ENSP00000471345.1:p.Thr62=
ENST00000601886.1:c.186C>T (ANGPTL4)	ENSP00000470307.1:p.Thr62=
NM_001039667.2:c.186C>T (ANGPTL4)	NP_001034756.1:p.Thr62=
NM_139314.2:c.186C>T (ANGPTL4)	NP_647475.1:p.Thr62=
NR_104213.1:n.381C>T (ANGPTL4)
XM_005272484.2:c.186C>T (ANGPTL4)	XP_005272541.1:p.Thr62=
XM_005272485.2:c.186C>T (ANGPTL4)	XP_005272542.1:p.Thr62=
XM_005272484.3:c.186C>T (ANGPTL4)	XP_005272541.1:p.Thr62=
XM_005272485.3:c.186C>T (ANGPTL4)	XP_005272542.1:p.Thr62=
NM_139314.3:c.186C>T (ANGPTL4) MANE Select	NP_647475.1:p.Thr62=
NM_001039667.3:c.186C>T (ANGPTL4)	NP_001034756.1:p.Thr62=
NR_104213.2:n.353C>T (ANGPTL4)