Canonical Allele Identifier: CA403721565

Gene: ANGPTL4 ELAVL1

Linked Data

• dbSNP Id: rs1599673003
• MyVariant Identifiers: chr19:g.8436170A>C (hg19) ; chr19:g.8371286A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8371286A>C , CM000681.2:g.8371286A>C	GRCh38
NC_000019.9:g.8436170A>C , CM000681.1:g.8436170A>C	GRCh37
NC_000019.8:g.8342170A>C	NCBI36
NG_012169.1:g.12160A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301455.7:c.803A>C (ANGPTL4) MANE Select	ENSP00000301455.1:p.Asp268Ala
ENST00000301455.6:c.803A>C (ANGPTL4)	ENSP00000301455.1:p.Asp268Ala
ENST00000351593.9:c.-88+73720T>G (ELAVL1)	ENSP00000264073.6:n.-88+73720T>G
ENST00000393962.6:c.689A>C (ANGPTL4)	ENSP00000377534.1:p.Asp230Ala
ENST00000593998.5:c.803A>C (ANGPTL4)	ENSP00000472551.1:p.Asp268Ala
ENST00000594875.1:c.354-2907A>C (ANGPTL4)
ENST00000595079.5:c.*346A>C (ANGPTL4)	ENSP00000473025.1:n.*346A>C
NM_001039667.2:c.689A>C (ANGPTL4)	NP_001034756.1:p.Asp230Ala
NM_139314.2:c.803A>C (ANGPTL4)	NP_647475.1:p.Asp268Ala
NR_104213.1:n.625-2907A>C (ANGPTL4)
XM_005272484.2:c.803A>C (ANGPTL4)	XP_005272541.1:p.Asp268Ala
XM_005272485.2:c.689A>C (ANGPTL4)	XP_005272542.1:p.Asp230Ala
XM_005272484.3:c.803A>C (ANGPTL4)	XP_005272541.1:p.Asp268Ala
XM_005272485.3:c.689A>C (ANGPTL4)	XP_005272542.1:p.Asp230Ala
NM_139314.3:c.803A>C (ANGPTL4) MANE Select	NP_647475.1:p.Asp268Ala
NM_001039667.3:c.689A>C (ANGPTL4)	NP_001034756.1:p.Asp230Ala
NR_104213.2:n.597-2907A>C (ANGPTL4)