Canonical Allele Identifier: CA2573130195

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21010178del , CM000664.2:g.21010178del	GRCh38
NC_000002.11:g.21233050del , CM000664.1:g.21233050del	GRCh37
NC_000002.10:g.21086555del	NCBI36
NG_011793.1:g.38898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.6692del MANE Select	ENSP00000233242.1:p.Leu2231CysfsTer?
ENST00000616098.4:c.6692del	ENSP00000477990.1:p.Leu2231CysfsTer?
NM_000384.2:c.6692del	NP_000375.2:p.Leu2231CysfsTer?
XM_011532809.1:c.5869+557del	XP_011531111.1:n.5869+557del
NM_000384.3:c.6692del MANE Select	NP_000375.3:p.Leu2231CysfsTer?