Canonical Allele Identifier: CA2338167033

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907108C= , CM000681.2:g.44907108C=	GRCh38
NC_000019.9:g.45410365C= , CM000681.1:g.45410365C=	GRCh37
NC_000019.8:g.50102205C=	NCBI36
NG_007084.2:g.6327C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.43+441C= MANE Select	ENSP00000252486.3:n.43+441C=
ENST00000252486.8:c.43+441C=	ENSP00000252486.3:n.43+441C=
ENST00000425718.1:c.43+441C=	ENSP00000410423.1:n.43+441C=
ENST00000434152.5:c.121+441C=	ENSP00000413653.2:n.121+441C=
ENST00000446996.5:c.43+441C=	ENSP00000413135.1:n.43+441C=
ENST00000485628.2:n.553C=
NM_000041.3:c.43+441C=	NP_000032.1:n.43+441C=
NM_001302688.1:c.121+441C=	NP_001289617.1:n.121+441C=
NM_001302689.1:c.43+441C=	NP_001289618.1:n.43+441C=
NM_001302690.1:c.43+441C=	NP_001289619.1:n.43+441C=
NM_001302691.1:c.43+441C=	NP_001289620.1:n.43+441C=
NM_000041.4:c.43+441C= MANE Select	NP_000032.1:n.43+441C=
NM_001302688.2:c.121+441C=	NP_001289617.1:n.121+441C=
NM_001302689.2:c.43+441C=	NP_001289618.1:n.43+441C=
NM_001302691.2:c.43+441C=	NP_001289620.1:n.43+441C=
NM_001302690.2:c.43+441C=	NP_001289619.1:n.43+441C=