Canonical Allele Identifier: CA2338167574
Gene: APOE HGNC NCBI

Linked Data

dbSNP Id: rs1969845690

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908147_44908148insAT , CM000681.2:g.44908147_44908148insAT GRCh38
NC_000019.9:g.45411404_45411405insAT , CM000681.1:g.45411404_45411405insAT GRCh37
NC_000019.8:g.50103244_50103245insAT NCBI36
NG_007084.2:g.7366_7367insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.236+195_236+196insAT MANE Select ENSP00000252486.3:n.236+195_236+196insAT
ENST00000252486.8:c.236+195_236+196insAT ENSP00000252486.3:n.236+195_236+196insAT
ENST00000425718.1:c.236+195_236+196insAT ENSP00000410423.1:n.236+195_236+196insAT
ENST00000434152.5:c.314+195_314+196insAT ENSP00000413653.2:n.314+195_314+196insAT
ENST00000446996.5:c.236+195_236+196insAT ENSP00000413135.1:n.236+195_236+196insAT
NM_000041.3:c.236+195_236+196insAT NP_000032.1:n.236+195_236+196insAT
NM_001302688.1:c.314+195_314+196insAT NP_001289617.1:n.314+195_314+196insAT
NM_001302689.1:c.236+195_236+196insAT NP_001289618.1:n.236+195_236+196insAT
NM_001302690.1:c.236+195_236+196insAT NP_001289619.1:n.236+195_236+196insAT
NM_001302691.1:c.236+195_236+196insAT NP_001289620.1:n.236+195_236+196insAT
NM_000041.4:c.236+195_236+196insAT MANE Select NP_000032.1:n.236+195_236+196insAT
NM_001302688.2:c.314+195_314+196insAT NP_001289617.1:n.314+195_314+196insAT
NM_001302689.2:c.236+195_236+196insAT NP_001289618.1:n.236+195_236+196insAT
NM_001302691.2:c.236+195_236+196insAT NP_001289620.1:n.236+195_236+196insAT
NM_001302690.2:c.236+195_236+196insAT NP_001289619.1:n.236+195_236+196insAT