Canonical Allele Identifier: CA2338167073

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907187_44907188delinsGT , CM000681.2:g.44907187_44907188delinsGT	GRCh38
NC_000019.9:g.45410444_45410445delinsGT , CM000681.1:g.45410444_45410445delinsGT	GRCh37
NC_000019.8:g.50102284_50102285delinsGT	NCBI36
NG_007084.2:g.6406_6407delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.43+520_43+521delinsGT MANE Select	ENSP00000252486.3:n.43+520_43+521delinsGT...
ENST00000252486.8:c.43+520_43+521delinsGT	ENSP00000252486.3:n.43+520_43+521delinsGT...
ENST00000425718.1:c.43+520_43+521delinsGT	ENSP00000410423.1:n.43+520_43+521delinsGT...
ENST00000434152.5:c.121+520_121+521delinsGT	ENSP00000413653.2:n.121+520_121+521delins...
ENST00000446996.5:c.43+520_43+521delinsGT	ENSP00000413135.1:n.43+520_43+521delinsGT...
ENST00000485628.2:n.632_633delinsGT
NM_000041.3:c.43+520_43+521delinsGT	NP_000032.1:n.43+520_43+521delinsGT
NM_001302688.1:c.121+520_121+521delinsGT	NP_001289617.1:n.121+520_121+521delinsGT
NM_001302689.1:c.43+520_43+521delinsGT	NP_001289618.1:n.43+520_43+521delinsGT
NM_001302690.1:c.43+520_43+521delinsGT	NP_001289619.1:n.43+520_43+521delinsGT
NM_001302691.1:c.43+520_43+521delinsGT	NP_001289620.1:n.43+520_43+521delinsGT
NM_000041.4:c.43+520_43+521delinsGT MANE Select	NP_000032.1:n.43+520_43+521delinsGT
NM_001302688.2:c.121+520_121+521delinsGT	NP_001289617.1:n.121+520_121+521delinsGT
NM_001302689.2:c.43+520_43+521delinsGT	NP_001289618.1:n.43+520_43+521delinsGT
NM_001302691.2:c.43+520_43+521delinsGT	NP_001289620.1:n.43+520_43+521delinsGT
NM_001302690.2:c.43+520_43+521delinsGT	NP_001289619.1:n.43+520_43+521delinsGT