Canonical Allele Identifier: CA9155945

Gene: ANGPTL4 ELAVL1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8366198del , CM000681.2:g.8366198del	GRCh38
NC_000019.9:g.8431082del , CM000681.1:g.8431082del	GRCh37
NC_000019.8:g.8337082del	NCBI36
NG_012169.1:g.7072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301455.7:c.430-4del (ANGPTL4) MANE Select	ENSP00000301455.1:n.430-4del
ENST00000301455.6:c.430-4del (ANGPTL4)	ENSP00000301455.1:n.430-4del
ENST00000351593.9:c.-88+78809del (ELAVL1)	ENSP00000264073.6:n.-88+78809del
ENST00000393962.6:c.430-4del (ANGPTL4)	ENSP00000377534.1:n.430-4del
ENST00000593998.5:c.430-4del (ANGPTL4)	ENSP00000472551.1:n.430-4del
ENST00000594348.1:n.583-4del (ANGPTL4)
ENST00000594875.1:c.353+134del (ANGPTL4)
ENST00000595079.5:c.360-4del (ANGPTL4)	ENSP00000473025.1:n.360-4del
ENST00000597137.5:n.176-4del (ANGPTL4)
ENST00000598255.5:n.586-4del (ANGPTL4)
NM_001039667.2:c.430-4del (ANGPTL4)	NP_001034756.1:n.430-4del
NM_139314.2:c.430-4del (ANGPTL4)	NP_647475.1:n.430-4del
NR_104213.1:n.624+134del (ANGPTL4)
XM_005272484.2:c.430-4del (ANGPTL4)	XP_005272541.1:n.430-4del
XM_005272485.2:c.430-4del (ANGPTL4)	XP_005272542.1:n.430-4del
XM_005272484.3:c.430-4del (ANGPTL4)	XP_005272541.1:n.430-4del
XM_005272485.3:c.430-4del (ANGPTL4)	XP_005272542.1:n.430-4del
NM_139314.3:c.430-4del (ANGPTL4) MANE Select	NP_647475.1:n.430-4del
NM_001039667.3:c.430-4del (ANGPTL4)	NP_001034756.1:n.430-4del
NR_104213.2:n.596+134del (ANGPTL4)