Canonical Allele Identifier: CA2338167684
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908743G= , CM000681.2:g.44908743G= GRCh38
NC_000019.9:g.45412000G= , CM000681.1:g.45412000G= GRCh37
NC_000019.8:g.50103840G= NCBI36
NG_007084.2:g.7962G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.447G= MANE Select ENSP00000252486.3:p.Glu149=
ENST00000252486.8:c.447G= ENSP00000252486.3:p.Glu149=
ENST00000425718.1:c.447G= ENSP00000410423.1:p.Glu149=
ENST00000434152.5:c.525G= ENSP00000413653.2:p.Glu175=
ENST00000446996.5:c.447G= ENSP00000413135.1:p.Glu149=
NM_000041.3:c.447G= NP_000032.1:p.Glu149=
NM_001302688.1:c.525G= NP_001289617.1:p.Glu175=
NM_001302689.1:c.447G= NP_001289618.1:p.Glu149=
NM_001302690.1:c.447G= NP_001289619.1:p.Glu149=
NM_001302691.1:c.447G= NP_001289620.1:p.Glu149=
NM_000041.4:c.447G= MANE Select NP_000032.1:p.Glu149=
NM_001302688.2:c.525G= NP_001289617.1:p.Glu175=
NM_001302689.2:c.447G= NP_001289618.1:p.Glu149=
NM_001302691.2:c.447G= NP_001289620.1:p.Glu149=
NM_001302690.2:c.447G= NP_001289619.1:p.Glu149=