Canonical Allele Identifier: CA2585713777

Gene: APOE

Linked Data

• gnomAD v4: 19-44905827-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905829del , CM000681.2:g.44905829del	GRCh38
NC_000019.9:g.45409086del , CM000681.1:g.45409086del	GRCh37
NC_000019.8:g.50100926del	NCBI36
NG_007084.2:g.5048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-36del MANE Select	ENSP00000252486.3:n.-36del
ENST00000252486.8:c.-36del	ENSP00000252486.3:n.-36del
ENST00000434152.5:c.-40del	ENSP00000413653.2:n.-40del
ENST00000446996.5:c.-51del	ENSP00000413135.1:n.-51del
ENST00000485628.2:n.34del
NM_000041.3:c.-36del	NP_000032.1:n.-36del
NM_001302688.1:c.-40del	NP_001289617.1:n.-40del
NM_001302691.1:c.-51del	NP_001289620.1:n.-51del
NM_000041.4:c.-36del MANE Select	NP_000032.1:n.-36del
NM_001302688.2:c.-40del	NP_001289617.1:n.-40del
NM_001302691.2:c.-51del	NP_001289620.1:n.-51del