Canonical Allele Identifier: CA2576686512
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007417del , CM000664.2:g.21007417del GRCh38
NC_000002.11:g.21230289del , CM000664.1:g.21230289del GRCh37
NC_000002.10:g.21083794del NCBI36
NG_011793.1:g.41657del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9451del MANE Select ENSP00000233242.1:p.Ser3151LeufsTer8
ENST00000616098.4:c.9451del ENSP00000477990.1:p.Ser3151LeufsTer8
NM_000384.2:c.9451del NP_000375.2:p.Ser3151LeufsTer8
XM_011532809.1:c.5869+3316del XP_011531111.1:n.5869+3316del
NM_000384.3:c.9451del MANE Select NP_000375.3:p.Ser3151LeufsTer8