Canonical Allele Identifier: CA2840288619

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023437dup , CM000664.2:g.21023437dup	GRCh38
NC_000002.11:g.21246309dup , CM000664.1:g.21246309dup	GRCh37
NC_000002.10:g.21099814dup	NCBI36
NG_011793.1:g.25638dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1910+89dup	ENSP00000501110.2:n.*1910+89dup
ENST00000673882.2:c.*1910+89dup	ENSP00000501253.2:n.*1910+89dup
ENST00000673739.1:c.2318+89dup	ENSP00000501110.1:n.2318+89dup
ENST00000673882.1:c.2318+89dup	ENSP00000501253.1:n.2318+89dup
ENST00000233242.5:c.2604+89dup MANE Select	ENSP00000233242.1:n.2604+89dup
ENST00000616098.4:c.2604+89dup	ENSP00000477990.1:n.2604+89dup
NM_000384.2:c.2604+89dup	NP_000375.2:n.2604+89dup
XM_011532809.1:c.2604+89dup	XP_011531111.1:n.2604+89dup
NM_000384.3:c.2604+89dup MANE Select	NP_000375.3:n.2604+89dup