Canonical Allele Identifier: CA2518015254
Gene: APOA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222334_161222335insTGGGAAAAGTAGGGGAGTA , CM000663.2:g.161222334_161222335insTGGGAAAAGTAGGGGAGTA GRCh38
NC_000001.10:g.161192124_161192125insTGGGAAAAGTAGGGGAGTA , CM000663.1:g.161192124_161192125insTGGGAAAAGTAGGGGAGTA GRCh37
NC_000001.9:g.159458748_159458749insTGGGAAAAGTAGGGGAGTA NCBI36
NG_012043.1:g.6294_6295insTACTCCCCTACTTTTCCCA

Transcript Alleles

HGVS Amino-acid change
ENST00000367990.7:c.*70_*71insTACTCCCCTACTTTTCCCA MANE Select ENSP00000356969.3:n.*70_*71insTACTCCCCTACTTTTCCCA
ENST00000463812.1:c.*70_*71insTACTCCCCTACTTTTCCCA ENSP00000476890.1:n.*70_*71insTACTCCCCTACTTTTCCCA
ENST00000464492.5:c.*70_*71insTACTCCCCTACTTTTCCCA ENSP00000476911.1:n.*70_*71insTACTCCCCTACTTTTCCCA
ENST00000468465.5:c.*70_*71insTACTCCCCTACTTTTCCCA ENSP00000476662.1:n.*70_*71insTACTCCCCTACTTTTCCCA
ENST00000470459.6:c.*70_*71insTACTCCCCTACTTTTCCCA ENSP00000477031.1:n.*70_*71insTACTCCCCTACTTTTCCCA
ENST00000481413.1:n.884_885insTACTCCCCTACTTTTCCCA
ENST00000481511.5:c.*370_*371insTACTCCCCTACTTTTCCCA ENSP00000477054.1:n.*370_*371insTACTCCCCTACTTTTCCCA
ENST00000491350.1:c.*156_*157insTACTCCCCTACTTTTCCCA ENSP00000477353.1:n.*156_*157insTACTCCCCTACTTTTCCCA
NM_001643.1:c.*70_*71insTACTCCCCTACTTTTCCCA NP_001634.1:n.*70_*71insTACTCCCCTACTTTTCCCA
NM_001643.2:c.*70_*71insTACTCCCCTACTTTTCCCA MANE Select NP_001634.1:n.*70_*71insTACTCCCCTACTTTTCCCA