Canonical Allele Identifier: CA2658056044
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011417_21011418insACT , CM000664.2:g.21011417_21011418insACT GRCh38
NC_000002.11:g.21234289_21234290insACT , CM000664.1:g.21234289_21234290insACT GRCh37
NC_000002.10:g.21087794_21087795insACT NCBI36
NG_011793.1:g.37657_37658insGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*4757_*4758insGTA ENSP00000501110.2:n.*4757_*4758insGTA
ENST00000673739.1:c.5165_5166insGTA ENSP00000501110.1:n.5165_5166insGTA
ENST00000233242.5:c.5451_5452insGTA MANE Select ENSP00000233242.1:p.Glu1817_Pro1818insVal
ENST00000616098.4:c.5451_5452insGTA ENSP00000477990.1:p.Glu1817_Pro1818insVal
NM_000384.2:c.5451_5452insGTA NP_000375.2:p.Glu1817_Pro1818insVal
XM_011532809.1:c.5451_5452insGTA XP_011531111.1:p.Glu1817_Pro1818insVal
NM_000384.3:c.5451_5452insGTA MANE Select NP_000375.3:p.Glu1817_Pro1818insVal