Canonical Allele Identifier: CA2493482691
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21023454_21023455delinsAT , CM000664.2:g.21023454_21023455delinsAT GRCh38
NC_000002.11:g.21246326_21246327delinsAT , CM000664.1:g.21246326_21246327delinsAT GRCh37
NC_000002.10:g.21099831_21099832delinsAT NCBI36
NG_011793.1:g.25619_25620delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*1910+70_*1910+71delinsAT ENSP00000501110.2:n.*1910+70_*1910+71deli...
ENST00000673882.2:c.*1910+70_*1910+71delinsAT ENSP00000501253.2:n.*1910+70_*1910+71deli...
ENST00000673739.1:c.2318+70_2318+71delinsAT ENSP00000501110.1:n.2318+70_2318+71delins...
ENST00000673882.1:c.2318+70_2318+71delinsAT ENSP00000501253.1:n.2318+70_2318+71delins...
ENST00000233242.5:c.2604+70_2604+71delinsAT MANE Select ENSP00000233242.1:n.2604+70_2604+71delins...
ENST00000616098.4:c.2604+70_2604+71delinsAT ENSP00000477990.1:n.2604+70_2604+71delins...
NM_000384.2:c.2604+70_2604+71delinsAT NP_000375.2:n.2604+70_2604+71delinsAT
XM_011532809.1:c.2604+70_2604+71delinsAT XP_011531111.1:n.2604+70_2604+71delinsAT
NM_000384.3:c.2604+70_2604+71delinsAT MANE Select NP_000375.3:n.2604+70_2604+71delinsAT