Canonical Allele Identifier: CA2002740692

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790658A= , CM000673.2:g.116790658A=	GRCh38
NC_000011.9:g.116661374A= , CM000673.1:g.116661374A=	GRCh37
NC_000011.8:g.116166584A=	NCBI36
NG_015894.1:g.6763T=
NG_015894.2:g.6763T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.571T= MANE Select	ENSP00000227665.4:p.Phe191=
ENST00000433069.2:c.571T=	ENSP00000399701.2:p.Phe191=
ENST00000673688.1:c.655T=	ENSP00000501141.1:p.Phe219=
ENST00000227665.8:c.571T=	ENSP00000227665.4:p.Phe191=
ENST00000542499.5:c.571T=	ENSP00000445002.1:p.Phe191=
NM_001166598.1:c.571T=	NP_001160070.1:p.Phe191=
NM_052968.4:c.571T=	NP_443200.2:p.Phe191=
NM_001166598.2:c.571T=	NP_001160070.1:p.Phe191=
NM_001371904.1:c.571T= MANE Select	NP_001358833.1:p.Phe191=
NM_052968.5:c.571T=	NP_443200.2:p.Phe191=