Canonical Allele Identifier: CA1202652322
Gene: APOA2 HGNC NCBI

Linked Data

dbSNP Id: rs1666184780

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222446_161222447insACAATAAATG , CM000663.2:g.161222446_161222447insACAATAAATG GRCh38
NC_000001.10:g.161192236_161192237insACAATAAATG , CM000663.1:g.161192236_161192237insACAATAAATG GRCh37
NC_000001.9:g.159458860_159458861insACAATAAATG NCBI36
NG_012043.1:g.6182_6183insCATTTATTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367990.7:c.261_262insCATTTATTGT MANE Select ENSP00000356969.3:p.Ser88HisfsTer4
ENST00000463273.5:c.261_262insCATTTATTGT ENSP00000476740.1:p.Ser88HisfsTer4
ENST00000463812.1:c.117_118insCATTTATTGT ENSP00000476890.1:p.Ser40HisfsTer4
ENST00000464492.5:c.360_361insCATTTATTGT ENSP00000476911.1:p.Ser121HisfsTer4
ENST00000468465.5:c.117_118insCATTTATTGT ENSP00000476662.1:p.Ser40HisfsTer4
ENST00000470459.6:c.207_208insCATTTATTGT ENSP00000477031.1:p.Ser70HisfsTer4
ENST00000481413.1:n.772_773insCATTTATTGT
ENST00000481511.5:c.*258_*259insCATTTATTGT ENSP00000477054.1:n.*258_*259insCATTTATTGT
ENST00000491350.1:c.*44_*45insCATTTATTGT ENSP00000477353.1:n.*44_*45insCATTTATTGT
NM_001643.1:c.261_262insCATTTATTGT NP_001634.1:p.Ser88HisfsTer4
NM_001643.2:c.261_262insCATTTATTGT MANE Select NP_001634.1:p.Ser88HisfsTer4