Canonical Allele Identifier: CA2338168054
Community Standard Title: NM_000041.4(APOE):c.787G= (p.Glu263=)
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909083G= , CM000681.2:g.44909083G= GRCh38
NC_000019.9:g.45412340G= , CM000681.1:g.45412340G= GRCh37
NC_000019.8:g.50104180G= NCBI36
NG_007084.2:g.8302G=

Transcript Alleles

HGVS Amino-acid Change
NM_000041.4:c.787G= MANE Select NP_000032.1:p.Glu263=
ENST00000252486.9:c.787G= MANE Select ENSP00000252486.3:p.Glu263=
NM_000041.3:c.787G= NP_000032.1:p.Glu263=
NM_001302688.1:c.865G= NP_001289617.1:p.Glu289=
NM_001302688.2:c.865G= NP_001289617.1:p.Glu289=
NM_001302689.1:c.787G= NP_001289618.1:p.Glu263=
NM_001302689.2:c.787G= NP_001289618.1:p.Glu263=
NM_001302690.1:c.787G= NP_001289619.1:p.Glu263=
NM_001302690.2:c.787G= NP_001289619.1:p.Glu263=
NM_001302691.1:c.787G= NP_001289620.1:p.Glu263=
NM_001302691.2:c.787G= NP_001289620.1:p.Glu263=
ENST00000252486.8:c.787G= ENSP00000252486.3:p.Glu263=