Canonical Allele Identifier: CA1202652329

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222459C= , CM000663.2:g.161222459C=	GRCh38
NC_000001.10:g.161192249C= , CM000663.1:g.161192249C=	GRCh37
NC_000001.9:g.159458873C=	NCBI36
NG_012043.1:g.6170G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.249G= MANE Select	ENSP00000356969.3:p.Leu83=
ENST00000463273.5:c.249G=	ENSP00000476740.1:p.Leu83=
ENST00000463812.1:c.105G=	ENSP00000476890.1:p.Leu35=
ENST00000464492.5:c.348G=	ENSP00000476911.1:p.Leu116=
ENST00000468465.5:c.105G=	ENSP00000476662.1:p.Leu35=
ENST00000470459.6:c.201-6G=	ENSP00000477031.1:n.201-6G=
ENST00000481413.1:n.760G=
ENST00000481511.5:c.*246G=	ENSP00000477054.1:n.*246G=
ENST00000491350.1:c.*32G=	ENSP00000477353.1:n.*32G=
NM_001643.1:c.249G=	NP_001634.1:p.Leu83=
NM_001643.2:c.249G= MANE Select	NP_001634.1:p.Leu83=