Canonical Allele Identifier: CA2002740689

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790654T= , CM000673.2:g.116790654T=	GRCh38
NC_000011.9:g.116661370T= , CM000673.1:g.116661370T=	GRCh37
NC_000011.8:g.116166580T=	NCBI36
NG_015894.1:g.6767A=
NG_015894.2:g.6767A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.575A= MANE Select	ENSP00000227665.4:p.His192=
ENST00000433069.2:c.575A=	ENSP00000399701.2:p.His192=
ENST00000673688.1:c.659A=	ENSP00000501141.1:p.His220=
ENST00000227665.8:c.575A=	ENSP00000227665.4:p.His192=
ENST00000542499.5:c.575A=	ENSP00000445002.1:p.His192=
NM_001166598.1:c.575A=	NP_001160070.1:p.His192=
NM_052968.4:c.575A=	NP_443200.2:p.His192=
NM_001166598.2:c.575A=	NP_001160070.1:p.His192=
NM_001371904.1:c.575A= MANE Select	NP_001358833.1:p.His192=
NM_052968.5:c.575A=	NP_443200.2:p.His192=