Canonical Allele Identifier: CA2002739797

Gene: APOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116790097G= , CM000673.2:g.116790097G=	GRCh38
NC_000011.9:g.116660813G= , CM000673.1:g.116660813G=	GRCh37
NC_000011.8:g.116166023G=	NCBI36
NG_015894.1:g.7324C=
NG_015894.2:g.7324C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001371904.1:c.*31C= MANE Select	NP_001358833.1:n.*31C=
ENST00000227665.9:c.*31C= MANE Select	ENSP00000227665.4:n.*31C=
NM_001166598.1:c.*31C=	NP_001160070.1:n.*31C=
NM_001166598.2:c.*31C=	NP_001160070.1:n.*31C=
NM_052968.4:c.*31C=	NP_443200.2:n.*31C=
NM_052968.5:c.*31C=	NP_443200.2:n.*31C=
ENST00000227665.8:c.*31C=	ENSP00000227665.4:n.*31C=
ENST00000433069.2:c.*31C=	ENSP00000399701.2:n.*31C=
ENST00000542499.5:c.*31C=	ENSP00000445002.1:n.*31C=
ENST00000673688.1:c.*31C=	ENSP00000501141.1:n.*31C=