Canonical Allele Identifier: CA9156055

Gene: ANGPTL4 ELAVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8371109C>T , CM000681.2:g.8371109C>T	GRCh38
NC_000019.9:g.8435993C>T , CM000681.1:g.8435993C>T	GRCh37
NC_000019.8:g.8341993C>T	NCBI36
NG_012169.1:g.11983C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301455.7:c.715C>T (ANGPTL4) MANE Select	ENSP00000301455.1:p.Arg239Trp
ENST00000301455.6:c.715C>T (ANGPTL4)	ENSP00000301455.1:p.Arg239Trp
ENST00000351593.9:c.-88+73897G>A (ELAVL1)	ENSP00000264073.6:n.-88+73897G>A
ENST00000393962.6:c.601C>T (ANGPTL4)	ENSP00000377534.1:p.Arg201Trp
ENST00000593998.5:c.715C>T (ANGPTL4)	ENSP00000472551.1:p.Arg239Trp
ENST00000594348.1:n.868C>T (ANGPTL4)
ENST00000594875.1:c.354-3084C>T (ANGPTL4)
ENST00000595079.5:c.*258C>T (ANGPTL4)	ENSP00000473025.1:n.*258C>T
ENST00000597137.5:n.461C>T (ANGPTL4)
ENST00000598255.5:n.757C>T (ANGPTL4)
NM_001039667.2:c.601C>T (ANGPTL4)	NP_001034756.1:p.Arg201Trp
NM_139314.2:c.715C>T (ANGPTL4)	NP_647475.1:p.Arg239Trp
NR_104213.1:n.625-3084C>T (ANGPTL4)
XM_005272484.2:c.715C>T (ANGPTL4)	XP_005272541.1:p.Arg239Trp
XM_005272485.2:c.601C>T (ANGPTL4)	XP_005272542.1:p.Arg201Trp
XM_005272484.3:c.715C>T (ANGPTL4)	XP_005272541.1:p.Arg239Trp
XM_005272485.3:c.601C>T (ANGPTL4)	XP_005272542.1:p.Arg201Trp
NM_139314.3:c.715C>T (ANGPTL4) MANE Select	NP_647475.1:p.Arg239Trp
NM_001039667.3:c.601C>T (ANGPTL4)	NP_001034756.1:p.Arg201Trp
NR_104213.2:n.597-3084C>T (ANGPTL4)