Canonical Allele Identifier: CA2338167545
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908115_44908117delinsTTC , CM000681.2:g.44908115_44908117delinsTTC GRCh38
NC_000019.9:g.45411372_45411374delinsTTC , CM000681.1:g.45411372_45411374delinsTTC GRCh37
NC_000019.8:g.50103212_50103214delinsTTC NCBI36
NG_007084.2:g.7334_7336delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.236+163_236+165delinsTTC MANE Select ENSP00000252486.3:n.236+163_236+165delinsTTC
ENST00000252486.8:c.236+163_236+165delinsTTC ENSP00000252486.3:n.236+163_236+165delinsTTC
ENST00000425718.1:c.236+163_236+165delinsTTC ENSP00000410423.1:n.236+163_236+165delinsTTC
ENST00000434152.5:c.314+163_314+165delinsTTC ENSP00000413653.2:n.314+163_314+165delinsTTC
ENST00000446996.5:c.236+163_236+165delinsTTC ENSP00000413135.1:n.236+163_236+165delinsTTC
NM_000041.3:c.236+163_236+165delinsTTC NP_000032.1:n.236+163_236+165delinsTTC
NM_001302688.1:c.314+163_314+165delinsTTC NP_001289617.1:n.314+163_314+165delinsTTC
NM_001302689.1:c.236+163_236+165delinsTTC NP_001289618.1:n.236+163_236+165delinsTTC
NM_001302690.1:c.236+163_236+165delinsTTC NP_001289619.1:n.236+163_236+165delinsTTC
NM_001302691.1:c.236+163_236+165delinsTTC NP_001289620.1:n.236+163_236+165delinsTTC
NM_000041.4:c.236+163_236+165delinsTTC MANE Select NP_000032.1:n.236+163_236+165delinsTTC
NM_001302688.2:c.314+163_314+165delinsTTC NP_001289617.1:n.314+163_314+165delinsTTC
NM_001302689.2:c.236+163_236+165delinsTTC NP_001289618.1:n.236+163_236+165delinsTTC
NM_001302691.2:c.236+163_236+165delinsTTC NP_001289620.1:n.236+163_236+165delinsTTC
NM_001302690.2:c.236+163_236+165delinsTTC NP_001289619.1:n.236+163_236+165delinsTTC