Canonical Allele Identifier: CA2002741156

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790957C= , CM000673.2:g.116790957C=	GRCh38
NC_000011.9:g.116661673C= , CM000673.1:g.116661673C=	GRCh37
NC_000011.8:g.116166883C=	NCBI36
NG_015894.1:g.6464G=
NG_015894.2:g.6464G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.272G= MANE Select	ENSP00000227665.4:p.Gly91=
ENST00000433069.2:c.272G=	ENSP00000399701.2:p.Gly91=
ENST00000673688.1:c.356G=	ENSP00000501141.1:p.Gly119=
ENST00000227665.8:c.272G=	ENSP00000227665.4:p.Gly91=
ENST00000433069.1:c.272G=	ENSP00000399701.1:p.Gly91=
ENST00000542499.5:c.272G=	ENSP00000445002.1:p.Gly91=
NM_001166598.1:c.272G=	NP_001160070.1:p.Gly91=
NM_052968.4:c.272G=	NP_443200.2:p.Gly91=
NM_001166598.2:c.272G=	NP_001160070.1:p.Gly91=
NM_001371904.1:c.272G= MANE Select	NP_001358833.1:p.Gly91=
NM_052968.5:c.272G=	NP_443200.2:p.Gly91=