Canonical Allele Identifier: CA31634138

Gene: APOA2

Linked Data

• dbSNP Id: rs865834629

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222414_161222415delinsAA , CM000663.2:g.161222414_161222415delinsAA	GRCh38
NC_000001.10:g.161192204_161192205delinsAA , CM000663.1:g.161192204_161192205delinsAA	GRCh37
NC_000001.9:g.159458828_159458829delinsAA	NCBI36
NG_012043.1:g.6214_6215delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.293_294delinsTT MANE Select	ENSP00000356969.3:p.Ala98Val
ENST00000463812.1:c.149_150delinsTT	ENSP00000476890.1:p.Ala50Val
ENST00000464492.5:c.392_393delinsTT	ENSP00000476911.1:p.Ala131Val
ENST00000468465.5:c.149_150delinsTT	ENSP00000476662.1:p.Ala50Val
ENST00000470459.6:c.239_240delinsTT	ENSP00000477031.1:p.Ala80Val
ENST00000481413.1:n.804_805delinsTT
ENST00000481511.5:c.*290_*291delinsTT	ENSP00000477054.1:n.*290_*291delinsTT
ENST00000491350.1:c.*76_*77delinsTT	ENSP00000477353.1:n.*76_*77delinsTT
NM_001643.1:c.293_294delinsTT	NP_001634.1:p.Ala98Val
NM_001643.2:c.293_294delinsTT MANE Select	NP_001634.1:p.Ala98Val