Canonical Allele Identifier: CA2002740789

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790700G= , CM000673.2:g.116790700G=	GRCh38
NC_000011.9:g.116661416G= , CM000673.1:g.116661416G=	GRCh37
NC_000011.8:g.116166626G=	NCBI36
NG_015894.1:g.6721C=
NG_015894.2:g.6721C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227665.9:c.529C= MANE Select	ENSP00000227665.4:p.Gln177=
ENST00000433069.2:c.529C=	ENSP00000399701.2:p.Gln177=
ENST00000673688.1:c.613C=	ENSP00000501141.1:p.Gln205=
ENST00000227665.8:c.529C=	ENSP00000227665.4:p.Gln177=
ENST00000542499.5:c.529C=	ENSP00000445002.1:p.Gln177=
NM_001166598.1:c.529C=	NP_001160070.1:p.Gln177=
NM_052968.4:c.529C=	NP_443200.2:p.Gln177=
NM_001166598.2:c.529C=	NP_001160070.1:p.Gln177=
NM_001371904.1:c.529C= MANE Select	NP_001358833.1:p.Gln177=
NM_052968.5:c.529C=	NP_443200.2:p.Gln177=