Canonical Allele Identifier: CA406303313

Gene: APOE

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907844G>C , CM000681.2:g.44907844G>C	GRCh38
NC_000019.9:g.45411101G>C , CM000681.1:g.45411101G>C	GRCh37
NC_000019.8:g.50102941G>C	NCBI36
NG_007084.2:g.7063G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.128G>C MANE Select	ENSP00000252486.3:p.Arg43Pro
ENST00000252486.8:c.128G>C	ENSP00000252486.3:p.Arg43Pro
ENST00000425718.1:c.128G>C	ENSP00000410423.1:p.Arg43Pro
ENST00000434152.5:c.206G>C	ENSP00000413653.2:p.Arg69Pro
ENST00000446996.5:c.128G>C	ENSP00000413135.1:p.Arg43Pro
NM_000041.3:c.128G>C	NP_000032.1:p.Arg43Pro
NM_001302688.1:c.206G>C	NP_001289617.1:p.Arg69Pro
NM_001302689.1:c.128G>C	NP_001289618.1:p.Arg43Pro
NM_001302690.1:c.128G>C	NP_001289619.1:p.Arg43Pro
NM_001302691.1:c.128G>C	NP_001289620.1:p.Arg43Pro
NM_000041.4:c.128G>C MANE Select	NP_000032.1:p.Arg43Pro
NM_001302688.2:c.206G>C	NP_001289617.1:p.Arg69Pro
NM_001302689.2:c.128G>C	NP_001289618.1:p.Arg43Pro
NM_001302691.2:c.128G>C	NP_001289620.1:p.Arg43Pro
NM_001302690.2:c.128G>C	NP_001289619.1:p.Arg43Pro