Canonical Allele Identifier: CA2338166458
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905931C= , CM000681.2:g.44905931C= GRCh38
NC_000019.9:g.45409188C= , CM000681.1:g.45409188C= GRCh37
NC_000019.8:g.50101028C= NCBI36
NG_007084.2:g.5150C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.-24+90C= MANE Select ENSP00000252486.3:n.-24+90C=
ENST00000252486.8:c.-24+90C= ENSP00000252486.3:n.-24+90C=
ENST00000434152.5:c.55+8C= ENSP00000413653.2:n.55+8C=
ENST00000446996.5:c.-39+90C= ENSP00000413135.1:n.-39+90C=
ENST00000485628.2:n.46+90C=
NM_000041.3:c.-24+90C= NP_000032.1:n.-24+90C=
NM_001302688.1:c.55+8C= NP_001289617.1:n.55+8C=
NM_001302691.1:c.-39+90C= NP_001289620.1:n.-39+90C=
NM_000041.4:c.-24+90C= MANE Select NP_000032.1:n.-24+90C=
NM_001302688.2:c.55+8C= NP_001289617.1:n.55+8C=
NM_001302691.2:c.-39+90C= NP_001289620.1:n.-39+90C=