Canonical Allele Identifier: CA2002741032

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790887C= , CM000673.2:g.116790887C=	GRCh38
NC_000011.9:g.116661603C= , CM000673.1:g.116661603C=	GRCh37
NC_000011.8:g.116166813C=	NCBI36
NG_015894.1:g.6534G=
NG_015894.2:g.6534G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.342G= MANE Select	ENSP00000227665.4:p.Ala114=
ENST00000433069.2:c.342G=	ENSP00000399701.2:p.Ala114=
ENST00000673688.1:c.426G=	ENSP00000501141.1:p.Ala142=
ENST00000227665.8:c.342G=	ENSP00000227665.4:p.Ala114=
ENST00000433069.1:c.342G=	ENSP00000399701.1:p.Ala114=
ENST00000542499.5:c.342G=	ENSP00000445002.1:p.Ala114=
NM_001166598.1:c.342G=	NP_001160070.1:p.Ala114=
NM_052968.4:c.342G=	NP_443200.2:p.Ala114=
NM_001166598.2:c.342G=	NP_001160070.1:p.Ala114=
NM_001371904.1:c.342G= MANE Select	NP_001358833.1:p.Ala114=
NM_052968.5:c.342G=	NP_443200.2:p.Ala114=