Canonical Allele Identifier: CA2002740962

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790801C= , CM000673.2:g.116790801C=	GRCh38
NC_000011.9:g.116661517C= , CM000673.1:g.116661517C=	GRCh37
NC_000011.8:g.116166727C=	NCBI36
NG_015894.1:g.6620G=
NG_015894.2:g.6620G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.428G= MANE Select	ENSP00000227665.4:p.Arg143=
ENST00000433069.2:c.428G=	ENSP00000399701.2:p.Arg143=
ENST00000673688.1:c.512G=	ENSP00000501141.1:p.Arg171=
ENST00000227665.8:c.428G=	ENSP00000227665.4:p.Arg143=
ENST00000433069.1:c.428G=	ENSP00000399701.1:p.Arg143=
ENST00000542499.5:c.428G=	ENSP00000445002.1:p.Arg143=
NM_001166598.1:c.428G=	NP_001160070.1:p.Arg143=
NM_052968.4:c.428G=	NP_443200.2:p.Arg143=
NM_001166598.2:c.428G=	NP_001160070.1:p.Arg143=
NM_001371904.1:c.428G= MANE Select	NP_001358833.1:p.Arg143=
NM_052968.5:c.428G=	NP_443200.2:p.Arg143=