Canonical Allele Identifier: CA308884362

Gene: APOE

Linked Data

• dbSNP Id: rs778638509
• gnomAD v3: 19-44907681-CCTT-C
• gnomAD v4: 19-44907681-CCTT-C
• MyVariant Identifiers: chr19:g.45410939_45410941del (hg19) ; chr19:g.44907682_44907684del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907684_44907686del , CM000681.2:g.44907684_44907686del	GRCh38
NC_000019.9:g.45410941_45410943del , CM000681.1:g.45410941_45410943del	GRCh37
NC_000019.8:g.50102781_50102783del	NCBI36
NG_007084.2:g.6903_6905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.44-76_44-74del MANE Select	ENSP00000252486.3:n.44-76_44-74del
ENST00000252486.8:c.44-76_44-74del	ENSP00000252486.3:n.44-76_44-74del
ENST00000425718.1:c.44-76_44-74del	ENSP00000410423.1:n.44-76_44-74del
ENST00000434152.5:c.122-76_122-74del	ENSP00000413653.2:n.122-76_122-74del
ENST00000446996.5:c.44-76_44-74del	ENSP00000413135.1:n.44-76_44-74del
NM_000041.3:c.44-76_44-74del	NP_000032.1:n.44-76_44-74del
NM_001302688.1:c.122-76_122-74del	NP_001289617.1:n.122-76_122-74del
NM_001302689.1:c.44-76_44-74del	NP_001289618.1:n.44-76_44-74del
NM_001302690.1:c.44-76_44-74del	NP_001289619.1:n.44-76_44-74del
NM_001302691.1:c.44-76_44-74del	NP_001289620.1:n.44-76_44-74del
NM_000041.4:c.44-76_44-74del MANE Select	NP_000032.1:n.44-76_44-74del
NM_001302688.2:c.122-76_122-74del	NP_001289617.1:n.122-76_122-74del
NM_001302689.2:c.44-76_44-74del	NP_001289618.1:n.44-76_44-74del
NM_001302691.2:c.44-76_44-74del	NP_001289620.1:n.44-76_44-74del
NM_001302690.2:c.44-76_44-74del	NP_001289619.1:n.44-76_44-74del