Canonical Allele Identifier: CA1028210356

Gene: APOB

Linked Data

• dbSNP Id: rs1664053065

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038257_21038258insAATAT , CM000664.2:g.21038257_21038258insAATAT	GRCh38
NC_000002.11:g.21261129_21261130insAATAT , CM000664.1:g.21261129_21261130insAATAT	GRCh37
NC_000002.10:g.21114634_21114635insAATAT	NCBI36
NG_011793.1:g.10816_10817insATATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1003_384-1002insATATT	ENSP00000501110.2:n.384-1003_384-1002insATATT
ENST00000673882.2:c.384-1003_384-1002insATATT	ENSP00000501253.2:n.384-1003_384-1002insATATT
ENST00000673739.1:c.252-1003_252-1002insATATT	ENSP00000501110.1:n.252-1003_252-1002insATATT
ENST00000673882.1:c.252-1003_252-1002insATATT	ENSP00000501253.1:n.252-1003_252-1002insATATT
ENST00000233242.5:c.384-147_384-146insATATT MANE Select	ENSP00000233242.1:n.384-147_384-146insATATT
ENST00000399256.4:c.384-147_384-146insATATT	ENSP00000382200.4:n.384-147_384-146insATATT
ENST00000616098.4:c.384-147_384-146insATATT	ENSP00000477990.1:n.384-147_384-146insATATT
NM_000384.2:c.384-147_384-146insATATT	NP_000375.2:n.384-147_384-146insATATT
XM_011532809.1:c.384-147_384-146insATATT	XP_011531111.1:n.384-147_384-146insATATT
NM_000384.3:c.384-147_384-146insATATT MANE Select	NP_000375.3:n.384-147_384-146insATATT