Canonical Allele Identifier: CA2749100376
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21043841_21043842del , CM000664.2:g.21043841_21043842del GRCh38
NC_000002.11:g.21266713_21266714del , CM000664.1:g.21266713_21266714del GRCh37
NC_000002.10:g.21120218_21120219del NCBI36
NG_011793.1:g.5233_5234del

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.82+23_82+24del ENSP00000501110.2:n.82+23_82+24del
ENST00000673882.2:c.82+23_82+24del ENSP00000501253.2:n.82+23_82+24del
ENST00000233242.5:c.82+23_82+24del MANE Select ENSP00000233242.1:n.82+23_82+24del
ENST00000399256.4:c.82+23_82+24del ENSP00000382200.4:n.82+23_82+24del
ENST00000616098.4:c.82+23_82+24del ENSP00000477990.1:n.82+23_82+24del
NM_000384.2:c.82+23_82+24del NP_000375.2:n.82+23_82+24del
XM_011532809.1:c.82+23_82+24del XP_011531111.1:n.82+23_82+24del
NM_000384.3:c.82+23_82+24del MANE Select NP_000375.3:n.82+23_82+24del
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