Canonical Allele Identifier: CA2741634406

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907956_44907957insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA , CM000681.2:g.44907956_44907957insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	GRCh38
NC_000019.9:g.45411213_45411214insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA , CM000681.1:g.45411213_45411214insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	GRCh37
NC_000019.8:g.50103053_50103054insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NCBI36
NG_007084.2:g.7175_7176insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA MANE Select	ENSP00000252486.3:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGG...
ENST00000252486.8:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	ENSP00000252486.3:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGG...
ENST00000425718.1:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	ENSP00000410423.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGG...
ENST00000434152.5:c.314+4_314+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	ENSP00000413653.2:n.314+4_314+5insTGGACGAGACCATGAAGGAGTTGAAGG...
ENST00000446996.5:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	ENSP00000413135.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGG...
NM_000041.3:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_000032.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACA...
NM_001302688.1:c.314+4_314+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289617.1:n.314+4_314+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...
NM_001302689.1:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289618.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...
NM_001302690.1:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289619.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...
NM_001302691.1:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289620.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...
NM_000041.4:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA MANE Select	NP_000032.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACA...
NM_001302688.2:c.314+4_314+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289617.1:n.314+4_314+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...
NM_001302689.2:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289618.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...
NM_001302691.2:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289620.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...
NM_001302690.2:c.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCTACAAATCGGAACTGGA	NP_001289619.1:n.236+4_236+5insTGGACGAGACCATGAAGGAGTTGAAGGCCT...