Canonical Allele Identifier: CA1202652321

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222447C= , CM000663.2:g.161222447C=	GRCh38
NC_000001.10:g.161192237C= , CM000663.1:g.161192237C=	GRCh37
NC_000001.9:g.159458861C=	NCBI36
NG_012043.1:g.6182G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.261G= MANE Select	ENSP00000356969.3:p.Leu87=
ENST00000463273.5:c.261G=	ENSP00000476740.1:p.Leu87=
ENST00000463812.1:c.117G=	ENSP00000476890.1:p.Leu39=
ENST00000464492.5:c.360G=	ENSP00000476911.1:p.Leu120=
ENST00000468465.5:c.117G=	ENSP00000476662.1:p.Leu39=
ENST00000470459.6:c.207G=	ENSP00000477031.1:p.Leu69=
ENST00000481413.1:n.772G=
ENST00000481511.5:c.*258G=	ENSP00000477054.1:n.*258G=
ENST00000491350.1:c.*44G=	ENSP00000477353.1:n.*44G=
NM_001643.1:c.261G=	NP_001634.1:p.Leu87=
NM_001643.2:c.261G= MANE Select	NP_001634.1:p.Leu87=