Canonical Allele Identifier: CA2338167606
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908205_44908207delinsTTA , CM000681.2:g.44908205_44908207delinsTTA GRCh38
NC_000019.9:g.45411462_45411464delinsTTA , CM000681.1:g.45411462_45411464delinsTTA GRCh37
NC_000019.8:g.50103302_50103304delinsTTA NCBI36
NG_007084.2:g.7424_7426delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.236+253_236+255delinsTTA MANE Select ENSP00000252486.3:n.236+253_236+255delinsTTA
ENST00000252486.8:c.236+253_236+255delinsTTA ENSP00000252486.3:n.236+253_236+255delinsTTA
ENST00000425718.1:c.236+253_236+255delinsTTA ENSP00000410423.1:n.236+253_236+255delinsTTA
ENST00000434152.5:c.314+253_314+255delinsTTA ENSP00000413653.2:n.314+253_314+255delinsTTA
ENST00000446996.5:c.236+253_236+255delinsTTA ENSP00000413135.1:n.236+253_236+255delinsTTA
NM_000041.3:c.236+253_236+255delinsTTA NP_000032.1:n.236+253_236+255delinsTTA
NM_001302688.1:c.314+253_314+255delinsTTA NP_001289617.1:n.314+253_314+255delinsTTA
NM_001302689.1:c.236+253_236+255delinsTTA NP_001289618.1:n.236+253_236+255delinsTTA
NM_001302690.1:c.236+253_236+255delinsTTA NP_001289619.1:n.236+253_236+255delinsTTA
NM_001302691.1:c.236+253_236+255delinsTTA NP_001289620.1:n.236+253_236+255delinsTTA
NM_000041.4:c.236+253_236+255delinsTTA MANE Select NP_000032.1:n.236+253_236+255delinsTTA
NM_001302688.2:c.314+253_314+255delinsTTA NP_001289617.1:n.314+253_314+255delinsTTA
NM_001302689.2:c.236+253_236+255delinsTTA NP_001289618.1:n.236+253_236+255delinsTTA
NM_001302691.2:c.236+253_236+255delinsTTA NP_001289620.1:n.236+253_236+255delinsTTA
NM_001302690.2:c.236+253_236+255delinsTTA NP_001289619.1:n.236+253_236+255delinsTTA