Canonical Allele Identifier: CA1202652280
Gene: APOA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222343_161222344delinsTA , CM000663.2:g.161222343_161222344delinsTA GRCh38
NC_000001.10:g.161192133_161192134delinsTA , CM000663.1:g.161192133_161192134delinsTA GRCh37
NC_000001.9:g.159458757_159458758delinsTA NCBI36
NG_012043.1:g.6285_6286delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367990.7:c.*61_*62delinsTA MANE Select ENSP00000356969.3:n.*61_*62delinsTA
ENST00000463812.1:c.*61_*62delinsTA ENSP00000476890.1:n.*61_*62delinsTA
ENST00000464492.5:c.*61_*62delinsTA ENSP00000476911.1:n.*61_*62delinsTA
ENST00000468465.5:c.*61_*62delinsTA ENSP00000476662.1:n.*61_*62delinsTA
ENST00000470459.6:c.*61_*62delinsTA ENSP00000477031.1:n.*61_*62delinsTA
ENST00000481413.1:n.875_876delinsTA
ENST00000481511.5:c.*361_*362delinsTA ENSP00000477054.1:n.*361_*362delinsTA
ENST00000491350.1:c.*147_*148delinsTA ENSP00000477353.1:n.*147_*148delinsTA
NM_001643.1:c.*61_*62delinsTA NP_001634.1:n.*61_*62delinsTA
NM_001643.2:c.*61_*62delinsTA MANE Select NP_001634.1:n.*61_*62delinsTA
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