Canonical Allele Identifier: CA2002739690

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116789977A= , CM000673.2:g.116789977A=	GRCh38
NC_000011.9:g.116660693A= , CM000673.1:g.116660693A=	GRCh37
NC_000011.8:g.116165903A=	NCBI36
NG_015894.1:g.7444T=
NG_015894.2:g.7444T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227665.9:c.*151T= MANE Select	ENSP00000227665.4:n.*151T=
ENST00000433069.2:c.*151T=	ENSP00000399701.2:n.*151T=
ENST00000227665.8:c.*151T=	ENSP00000227665.4:n.*151T=
ENST00000542499.5:c.*151T=	ENSP00000445002.1:n.*151T=
NM_001166598.1:c.*151T=	NP_001160070.1:n.*151T=
NM_052968.4:c.*151T=	NP_443200.2:n.*151T=
NM_001166598.2:c.*151T=	NP_001160070.1:n.*151T=
NM_001371904.1:c.*151T= MANE Select	NP_001358833.1:n.*151T=
NM_052968.5:c.*151T=	NP_443200.2:n.*151T=