Canonical Allele Identifier: CA2338167884

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908791_44908794delinsGCTC , CM000681.2:g.44908791_44908794delinsGCTC	GRCh38
NC_000019.9:g.45412048_45412051delinsGCTC , CM000681.1:g.45412048_45412051delinsGCTC	GRCh37
NC_000019.8:g.50103888_50103891delinsGCTC	NCBI36
NG_007084.2:g.8010_8013delinsGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.495_498delinsGCTC MANE Select	ENSP00000252486.3:p.Arg165=
ENST00000252486.8:c.495_498delinsGCTC	ENSP00000252486.3:p.Arg165=
ENST00000425718.1:c.495_498delinsGCTC	ENSP00000410423.1:p.Arg165=
ENST00000434152.5:c.573_576delinsGCTC	ENSP00000413653.2:p.Arg191=
ENST00000446996.5:c.495_498delinsGCTC	ENSP00000413135.1:p.Arg165=
NM_000041.3:c.495_498delinsGCTC	NP_000032.1:p.Arg165=
NM_001302688.1:c.573_576delinsGCTC	NP_001289617.1:p.Arg191=
NM_001302689.1:c.495_498delinsGCTC	NP_001289618.1:p.Arg165=
NM_001302690.1:c.495_498delinsGCTC	NP_001289619.1:p.Arg165=
NM_001302691.1:c.495_498delinsGCTC	NP_001289620.1:p.Arg165=
NM_000041.4:c.495_498delinsGCTC MANE Select	NP_000032.1:p.Arg165=
NM_001302688.2:c.573_576delinsGCTC	NP_001289617.1:p.Arg191=
NM_001302689.2:c.495_498delinsGCTC	NP_001289618.1:p.Arg165=
NM_001302691.2:c.495_498delinsGCTC	NP_001289620.1:p.Arg165=
NM_001302690.2:c.495_498delinsGCTC	NP_001289619.1:p.Arg165=