Canonical Allele Identifier: CA9505982
Gene: APOE HGNC NCBI

Linked Data

dbSNP Id: rs768374191

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44907844_44907858del , CM000681.2:g.44907844_44907858del GRCh38
NC_000019.9:g.45411101_45411115del , CM000681.1:g.45411101_45411115del GRCh37
NC_000019.8:g.50102941_50102955del NCBI36
NG_007084.2:g.7063_7077del

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.128_142del MANE Select ENSP00000252486.3:p.Arg43_Ala47del
ENST00000252486.8:c.128_142del ENSP00000252486.3:p.Arg43_Ala47del
ENST00000425718.1:c.128_142del ENSP00000410423.1:p.Arg43_Ala47del
ENST00000434152.5:c.206_220del ENSP00000413653.2:p.Arg69_Ala73del
ENST00000446996.5:c.128_142del ENSP00000413135.1:p.Arg43_Ala47del
NM_000041.3:c.128_142del NP_000032.1:p.Arg43_Ala47del
NM_001302688.1:c.206_220del NP_001289617.1:p.Arg69_Ala73del
NM_001302689.1:c.128_142del NP_001289618.1:p.Arg43_Ala47del
NM_001302690.1:c.128_142del NP_001289619.1:p.Arg43_Ala47del
NM_001302691.1:c.128_142del NP_001289620.1:p.Arg43_Ala47del
NM_000041.4:c.128_142del MANE Select NP_000032.1:p.Arg43_Ala47del
NM_001302688.2:c.206_220del NP_001289617.1:p.Arg69_Ala73del
NM_001302689.2:c.128_142del NP_001289618.1:p.Arg43_Ala47del
NM_001302691.2:c.128_142del NP_001289620.1:p.Arg43_Ala47del
NM_001302690.2:c.128_142del NP_001289619.1:p.Arg43_Ala47del