Canonical Allele Identifier: CA2002741176

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790966_116790984delinsTCCTGTGGGAGCCGAGGAG , CM000673.2:g.116790966_116790984delinsTCCTGTGGGAGCCGAGGAG	GRCh38
NC_000011.9:g.116661682_116661700delinsTCCTGTGGGAGCCGAGGAG , CM000673.1:g.116661682_116661700delinsTCCTGTGGGAGCCGAGGAG	GRCh37
NC_000011.8:g.116166892_116166910delinsTCCTGTGGGAGCCGAGGAG	NCBI36
NG_015894.1:g.6437_6455delinsCTCCTCGGCTCCCACAGGA
NG_015894.2:g.6437_6455delinsCTCCTCGGCTCCCACAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.245_263delinsCTCCTCGGCTCCCACAGGA MANE Select	ENSP00000227665.4:p.Ala82=
ENST00000433069.2:c.245_263delinsCTCCTCGGCTCCCACAGGA	ENSP00000399701.2:p.Ala82=
ENST00000673688.1:c.329_347delinsCTCCTCGGCTCCCACAGGA	ENSP00000501141.1:p.Ala110=
ENST00000227665.8:c.245_263delinsCTCCTCGGCTCCCACAGGA	ENSP00000227665.4:p.Ala82=
ENST00000433069.1:c.245_263delinsCTCCTCGGCTCCCACAGGA	ENSP00000399701.1:p.Ala82=
ENST00000542499.5:c.245_263delinsCTCCTCGGCTCCCACAGGA	ENSP00000445002.1:p.Ala82=
NM_001166598.1:c.245_263delinsCTCCTCGGCTCCCACAGGA	NP_001160070.1:p.Ala82=
NM_052968.4:c.245_263delinsCTCCTCGGCTCCCACAGGA	NP_443200.2:p.Ala82=
NM_001166598.2:c.245_263delinsCTCCTCGGCTCCCACAGGA	NP_001160070.1:p.Ala82=
NM_001371904.1:c.245_263delinsCTCCTCGGCTCCCACAGGA MANE Select	NP_001358833.1:p.Ala82=
NM_052968.5:c.245_263delinsCTCCTCGGCTCCCACAGGA	NP_443200.2:p.Ala82=