Canonical Allele Identifier: CA2321388184

Gene: ANGPTL4 ELAVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8373832G= , CM000681.2:g.8373832G=	GRCh38
NC_000019.9:g.8438716G= , CM000681.1:g.8438716G=	GRCh37
NC_000019.8:g.8344716G=	NCBI36
NG_012169.1:g.14706G=

Transcript Alleles

HGVS	Amino-acid Change
NM_139314.3:c.1167G= (ANGPTL4) MANE Select	NP_647475.1:p.Pro389=
ENST00000301455.7:c.1167G= (ANGPTL4) MANE Select	ENSP00000301455.1:p.Pro389=
NM_001039667.2:c.1053G= (ANGPTL4)	NP_001034756.1:p.Pro351=
NM_001039667.3:c.1053G= (ANGPTL4)	NP_001034756.1:p.Pro351=
NM_139314.2:c.1167G= (ANGPTL4)	NP_647475.1:p.Pro389=
NR_104213.1:n.625-361G= (ANGPTL4)
NR_104213.2:n.597-361G= (ANGPTL4)
ENST00000301455.6:c.1167G= (ANGPTL4)	ENSP00000301455.1:p.Pro389=
ENST00000351593.9:c.-88+71174C= (ELAVL1)	ENSP00000264073.6:n.-88+71174C=
ENST00000393962.6:c.1053G= (ANGPTL4)	ENSP00000377534.1:p.Pro351=
ENST00000593998.5:c.1167G= (ANGPTL4)	ENSP00000472551.1:p.Pro389=
ENST00000594875.1:c.354-361G= (ANGPTL4)
ENST00000595079.5:c.*710G= (ANGPTL4)	ENSP00000473025.1:n.*710G=
XM_005272484.2:c.1221G= (ANGPTL4)	XP_005272541.1:p.Pro407=
XM_005272484.3:c.1221G= (ANGPTL4)	XP_005272541.1:p.Pro407=
XM_005272485.2:c.1107G= (ANGPTL4)	XP_005272542.1:p.Pro369=
XM_005272485.3:c.1107G= (ANGPTL4)	XP_005272542.1:p.Pro369=