Canonical Allele Identifier: CA2338167856
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908586_44908587delinsAG , CM000681.2:g.44908586_44908587delinsAG GRCh38
NC_000019.9:g.45411843_45411844delinsAG , CM000681.1:g.45411843_45411844delinsAG GRCh37
NC_000019.8:g.50103683_50103684delinsAG NCBI36
NG_007084.2:g.7805_7806delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.290_291delinsAG MANE Select ENSP00000252486.3:p.Glu97=
ENST00000252486.8:c.290_291delinsAG ENSP00000252486.3:p.Glu97=
ENST00000425718.1:c.290_291delinsAG ENSP00000410423.1:p.Glu97=
ENST00000434152.5:c.368_369delinsAG ENSP00000413653.2:p.Glu123=
ENST00000446996.5:c.290_291delinsAG ENSP00000413135.1:p.Glu97=
NM_000041.3:c.290_291delinsAG NP_000032.1:p.Glu97=
NM_001302688.1:c.368_369delinsAG NP_001289617.1:p.Glu123=
NM_001302689.1:c.290_291delinsAG NP_001289618.1:p.Glu97=
NM_001302690.1:c.290_291delinsAG NP_001289619.1:p.Glu97=
NM_001302691.1:c.290_291delinsAG NP_001289620.1:p.Glu97=
NM_000041.4:c.290_291delinsAG MANE Select NP_000032.1:p.Glu97=
NM_001302688.2:c.368_369delinsAG NP_001289617.1:p.Glu123=
NM_001302689.2:c.290_291delinsAG NP_001289618.1:p.Glu97=
NM_001302691.2:c.290_291delinsAG NP_001289620.1:p.Glu97=
NM_001302690.2:c.290_291delinsAG NP_001289619.1:p.Glu97=