Canonical Allele Identifier: CA2695228862
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908705_44908706insATTCGACGTCACA , CM000681.2:g.44908705_44908706insATTCGACGTCACA GRCh38
NC_000019.9:g.45411962_45411963insATTCGACGTCACA , CM000681.1:g.45411962_45411963insATTCGACGTCACA GRCh37
NC_000019.8:g.50103802_50103803insATTCGACGTCACA NCBI36
NG_007084.2:g.7924_7925insATTCGACGTCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.409_410insATTCGACGTCACA MANE Select ENSP00000252486.3:p.Arg137HisfsTer32
ENST00000252486.8:c.409_410insATTCGACGTCACA ENSP00000252486.3:p.Arg137HisfsTer32
ENST00000425718.1:c.409_410insATTCGACGTCACA ENSP00000410423.1:p.Arg137HisfsTer32
ENST00000434152.5:c.487_488insATTCGACGTCACA ENSP00000413653.2:p.Arg163HisfsTer32
ENST00000446996.5:c.409_410insATTCGACGTCACA ENSP00000413135.1:p.Arg137HisfsTer32
NM_000041.3:c.409_410insATTCGACGTCACA NP_000032.1:p.Arg137HisfsTer32
NM_001302688.1:c.487_488insATTCGACGTCACA NP_001289617.1:p.Arg163HisfsTer32
NM_001302689.1:c.409_410insATTCGACGTCACA NP_001289618.1:p.Arg137HisfsTer32
NM_001302690.1:c.409_410insATTCGACGTCACA NP_001289619.1:p.Arg137HisfsTer32
NM_001302691.1:c.409_410insATTCGACGTCACA NP_001289620.1:p.Arg137HisfsTer32
NM_000041.4:c.409_410insATTCGACGTCACA MANE Select NP_000032.1:p.Arg137HisfsTer32
NM_001302688.2:c.487_488insATTCGACGTCACA NP_001289617.1:p.Arg163HisfsTer32
NM_001302689.2:c.409_410insATTCGACGTCACA NP_001289618.1:p.Arg137HisfsTer32
NM_001302691.2:c.409_410insATTCGACGTCACA NP_001289620.1:p.Arg137HisfsTer32
NM_001302690.2:c.409_410insATTCGACGTCACA NP_001289619.1:p.Arg137HisfsTer32