Canonical Allele Identifier: CA2002739758

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790062T= , CM000673.2:g.116790062T=	GRCh38
NC_000011.9:g.116660778T= , CM000673.1:g.116660778T=	GRCh37
NC_000011.8:g.116165988T=	NCBI36
NG_015894.1:g.7359A=
NG_015894.2:g.7359A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227665.9:c.*66A= MANE Select	ENSP00000227665.4:n.*66A=
ENST00000433069.2:c.*66A=	ENSP00000399701.2:n.*66A=
ENST00000227665.8:c.*66A=	ENSP00000227665.4:n.*66A=
ENST00000542499.5:c.*66A=	ENSP00000445002.1:n.*66A=
NM_001166598.1:c.*66A=	NP_001160070.1:n.*66A=
NM_052968.4:c.*66A=	NP_443200.2:n.*66A=
NM_001166598.2:c.*66A=	NP_001160070.1:n.*66A=
NM_001371904.1:c.*66A= MANE Select	NP_001358833.1:n.*66A=
NM_052968.5:c.*66A=	NP_443200.2:n.*66A=