Canonical Allele Identifier: CA2586968878

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011003del , CM000664.2:g.21011003del	GRCh38
NC_000002.11:g.21233875del , CM000664.1:g.21233875del	GRCh37
NC_000002.10:g.21087380del	NCBI36
NG_011793.1:g.38071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5865del MANE Select	ENSP00000233242.1:p.Ser1956LeufsTer?
ENST00000616098.4:c.5865del	ENSP00000477990.1:p.Ser1956LeufsTer?
NM_000384.2:c.5865del	NP_000375.2:p.Ser1956LeufsTer?
XM_011532809.1:c.5864+1del	XP_011531111.1:n.5864+1del
NM_000384.3:c.5865del MANE Select	NP_000375.3:p.Ser1956LeufsTer?