Canonical Allele Identifier: CA2002739864

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790192T= , CM000673.2:g.116790192T=	GRCh38
NC_000011.9:g.116660908T= , CM000673.1:g.116660908T=	GRCh37
NC_000011.8:g.116166118T=	NCBI36
NG_015894.1:g.7229A=
NG_015894.2:g.7229A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.1037A= MANE Select	ENSP00000227665.4:p.Asp346=
ENST00000433069.2:c.1037A=	ENSP00000399701.2:p.Asp346=
ENST00000673688.1:c.1121A=	ENSP00000501141.1:p.Asp374=
ENST00000227665.8:c.1037A=	ENSP00000227665.4:p.Asp346=
ENST00000542499.5:c.1037A=	ENSP00000445002.1:p.Asp346=
NM_001166598.1:c.1037A=	NP_001160070.1:p.Asp346=
NM_052968.4:c.1037A=	NP_443200.2:p.Asp346=
NM_001166598.2:c.1037A=	NP_001160070.1:p.Asp346=
NM_001371904.1:c.1037A= MANE Select	NP_001358833.1:p.Asp346=
NM_052968.5:c.1037A=	NP_443200.2:p.Asp346=