Canonical Allele Identifier: CA2658048731

Gene: APOB

Linked Data

• gnomAD v4: 2-21037875-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037876del , CM000664.2:g.21037876del	GRCh38
NC_000002.11:g.21260748del , CM000664.1:g.21260748del	GRCh37
NC_000002.10:g.21114253del	NCBI36
NG_011793.1:g.11198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-621del	ENSP00000501110.2:n.384-621del
ENST00000673882.2:c.384-621del	ENSP00000501253.2:n.384-621del
ENST00000673739.1:c.252-621del	ENSP00000501110.1:n.252-621del
ENST00000673882.1:c.252-621del	ENSP00000501253.1:n.252-621del
ENST00000233242.5:c.537+82del MANE Select	ENSP00000233242.1:n.537+82del
ENST00000399256.4:c.537+82del	ENSP00000382200.4:n.537+82del
ENST00000616098.4:c.537+82del	ENSP00000477990.1:n.537+82del
NM_000384.2:c.537+82del	NP_000375.2:n.537+82del
XM_011532809.1:c.537+82del	XP_011531111.1:n.537+82del
NM_000384.3:c.537+82del MANE Select	NP_000375.3:n.537+82del