Canonical Allele Identifier: CA2338167561
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908132_44908143delinsGTCTCTCTCTCT , CM000681.2:g.44908132_44908143delinsGTCTCTCTCTCT GRCh38
NC_000019.9:g.45411389_45411400delinsGTCTCTCTCTCT , CM000681.1:g.45411389_45411400delinsGTCTCTCTCTCT GRCh37
NC_000019.8:g.50103229_50103240delinsGTCTCTCTCTCT NCBI36
NG_007084.2:g.7351_7362delinsGTCTCTCTCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.236+180_236+191delinsGTCTCTCTCTCT MANE Select ENSP00000252486.3:n.236+180_236+191delinsGTCTCTCTCTCT
ENST00000252486.8:c.236+180_236+191delinsGTCTCTCTCTCT ENSP00000252486.3:n.236+180_236+191delinsGTCTCTCTCTCT
ENST00000425718.1:c.236+180_236+191delinsGTCTCTCTCTCT ENSP00000410423.1:n.236+180_236+191delinsGTCTCTCTCTCT
ENST00000434152.5:c.314+180_314+191delinsGTCTCTCTCTCT ENSP00000413653.2:n.314+180_314+191delinsGTCTCTCTCTCT
ENST00000446996.5:c.236+180_236+191delinsGTCTCTCTCTCT ENSP00000413135.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_000041.3:c.236+180_236+191delinsGTCTCTCTCTCT NP_000032.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_001302688.1:c.314+180_314+191delinsGTCTCTCTCTCT NP_001289617.1:n.314+180_314+191delinsGTCTCTCTCTCT
NM_001302689.1:c.236+180_236+191delinsGTCTCTCTCTCT NP_001289618.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_001302690.1:c.236+180_236+191delinsGTCTCTCTCTCT NP_001289619.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_001302691.1:c.236+180_236+191delinsGTCTCTCTCTCT NP_001289620.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_000041.4:c.236+180_236+191delinsGTCTCTCTCTCT MANE Select NP_000032.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_001302688.2:c.314+180_314+191delinsGTCTCTCTCTCT NP_001289617.1:n.314+180_314+191delinsGTCTCTCTCTCT
NM_001302689.2:c.236+180_236+191delinsGTCTCTCTCTCT NP_001289618.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_001302691.2:c.236+180_236+191delinsGTCTCTCTCTCT NP_001289620.1:n.236+180_236+191delinsGTCTCTCTCTCT
NM_001302690.2:c.236+180_236+191delinsGTCTCTCTCTCT NP_001289619.1:n.236+180_236+191delinsGTCTCTCTCTCT