Canonical Allele Identifier: CA657468976

Gene: APOE

Linked Data

• COSMIC: COSN16417902

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905831_44905832insT , CM000681.2:g.44905831_44905832insT	GRCh38
NC_000019.9:g.45409088_45409089insT , CM000681.1:g.45409088_45409089insT	GRCh37
NC_000019.8:g.50100928_50100929insT	NCBI36
NG_007084.2:g.5050_5051insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-34_-33insT MANE Select	ENSP00000252486.3:n.-34_-33insT
ENST00000252486.8:c.-34_-33insT	ENSP00000252486.3:n.-34_-33insT
ENST00000434152.5:c.-38_-37insT	ENSP00000413653.2:n.-38_-37insT
ENST00000446996.5:c.-49_-48insT	ENSP00000413135.1:n.-49_-48insT
ENST00000485628.2:n.36_37insT
NM_000041.3:c.-34_-33insT	NP_000032.1:n.-34_-33insT
NM_001302688.1:c.-38_-37insT	NP_001289617.1:n.-38_-37insT
NM_001302691.1:c.-49_-48insT	NP_001289620.1:n.-49_-48insT
NM_000041.4:c.-34_-33insT MANE Select	NP_000032.1:n.-34_-33insT
NM_001302688.2:c.-38_-37insT	NP_001289617.1:n.-38_-37insT
NM_001302691.2:c.-49_-48insT	NP_001289620.1:n.-49_-48insT