Canonical Allele Identifier: CA1202652335

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222478T= , CM000663.2:g.161222478T=	GRCh38
NC_000001.10:g.161192268T= , CM000663.1:g.161192268T=	GRCh37
NC_000001.9:g.159458892T=	NCBI36
NG_012043.1:g.6151A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.230A= MANE Select	ENSP00000356969.3:p.Lys77=
ENST00000463273.5:c.230A=	ENSP00000476740.1:p.Lys77=
ENST00000463812.1:c.86A=	ENSP00000476890.1:p.Lys29=
ENST00000464492.5:c.329A=	ENSP00000476911.1:p.Lys110=
ENST00000468465.5:c.86A=	ENSP00000476662.1:p.Lys29=
ENST00000470459.6:c.201-25A=	ENSP00000477031.1:n.201-25A=
ENST00000481413.1:n.741A=
ENST00000481511.5:c.*227A=	ENSP00000477054.1:n.*227A=
ENST00000491350.1:c.*13A=	ENSP00000477353.1:n.*13A=
NM_001643.1:c.230A=	NP_001634.1:p.Lys77=
NM_001643.2:c.230A= MANE Select	NP_001634.1:p.Lys77=