Canonical Allele Identifier: CA2338166447
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905917C= , CM000681.2:g.44905917C= GRCh38
NC_000019.9:g.45409174C= , CM000681.1:g.45409174C= GRCh37
NC_000019.8:g.50101014C= NCBI36
NG_007084.2:g.5136C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.-24+76C= MANE Select ENSP00000252486.3:n.-24+76C=
ENST00000252486.8:c.-24+76C= ENSP00000252486.3:n.-24+76C=
ENST00000434152.5:c.49C= ENSP00000413653.2:p.Pro17=
ENST00000446996.5:c.-39+76C= ENSP00000413135.1:n.-39+76C=
ENST00000485628.2:n.46+76C=
NM_000041.3:c.-24+76C= NP_000032.1:n.-24+76C=
NM_001302688.1:c.49C= NP_001289617.1:p.Pro17=
NM_001302691.1:c.-39+76C= NP_001289620.1:n.-39+76C=
NM_000041.4:c.-24+76C= MANE Select NP_000032.1:n.-24+76C=
NM_001302688.2:c.49C= NP_001289617.1:p.Pro17=
NM_001302691.2:c.-39+76C= NP_001289620.1:n.-39+76C=