Canonical Allele Identifier: CA1202652323

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222449_161222450delinsAG , CM000663.2:g.161222449_161222450delinsAG	GRCh38
NC_000001.10:g.161192239_161192240delinsAG , CM000663.1:g.161192239_161192240delinsAG	GRCh37
NC_000001.9:g.159458863_159458864delinsAG	NCBI36
NG_012043.1:g.6179_6180delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.258_259delinsCT MANE Select	ENSP00000356969.3:p.Phe86=
ENST00000463273.5:c.258_259delinsCT	ENSP00000476740.1:p.Phe86=
ENST00000463812.1:c.114_115delinsCT	ENSP00000476890.1:p.Phe38=
ENST00000464492.5:c.357_358delinsCT	ENSP00000476911.1:p.Phe119=
ENST00000468465.5:c.114_115delinsCT	ENSP00000476662.1:p.Phe38=
ENST00000470459.6:c.204_205delinsCT	ENSP00000477031.1:p.Phe68=
ENST00000481413.1:n.769_770delinsCT
ENST00000481511.5:c.*255_*256delinsCT	ENSP00000477054.1:n.*255_*256delinsCT
ENST00000491350.1:c.*41_*42delinsCT	ENSP00000477353.1:n.*41_*42delinsCT
NM_001643.1:c.258_259delinsCT	NP_001634.1:p.Phe86=
NM_001643.2:c.258_259delinsCT MANE Select	NP_001634.1:p.Phe86=