Canonical Allele Identifier: CA406304144

Gene: APOE

Linked Data

• MyVariant Identifiers: chr19:g.45412059A>C (hg19) ; chr19:g.44908802A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908802A>C , CM000681.2:g.44908802A>C	GRCh38
NC_000019.9:g.45412059A>C , CM000681.1:g.45412059A>C	GRCh37
NC_000019.8:g.50103899A>C	NCBI36
NG_007084.2:g.8021A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.506A>C MANE Select	ENSP00000252486.3:p.Asp169Ala
ENST00000252486.8:c.506A>C	ENSP00000252486.3:p.Asp169Ala
ENST00000425718.1:c.506A>C	ENSP00000410423.1:p.Asp169Ala
ENST00000434152.5:c.584A>C	ENSP00000413653.2:p.Asp195Ala
ENST00000446996.5:c.506A>C	ENSP00000413135.1:p.Asp169Ala
NM_000041.3:c.506A>C	NP_000032.1:p.Asp169Ala
NM_001302688.1:c.584A>C	NP_001289617.1:p.Asp195Ala
NM_001302689.1:c.506A>C	NP_001289618.1:p.Asp169Ala
NM_001302690.1:c.506A>C	NP_001289619.1:p.Asp169Ala
NM_001302691.1:c.506A>C	NP_001289620.1:p.Asp169Ala
NM_000041.4:c.506A>C MANE Select	NP_000032.1:p.Asp169Ala
NM_001302688.2:c.584A>C	NP_001289617.1:p.Asp195Ala
NM_001302689.2:c.506A>C	NP_001289618.1:p.Asp169Ala
NM_001302691.2:c.506A>C	NP_001289620.1:p.Asp169Ala
NM_001302690.2:c.506A>C	NP_001289619.1:p.Asp169Ala