Canonical Allele Identifier: CA2493472600

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21001775_21001776delinsGT , CM000664.2:g.21001775_21001776delinsGT	GRCh38
NC_000002.11:g.21224647_21224648delinsGT , CM000664.1:g.21224647_21224648delinsGT	GRCh37
NC_000002.10:g.21078152_21078153delinsGT	NCBI36
NG_011793.1:g.47298_47299delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.13646_13647delinsAC MANE Select	ENSP00000233242.1:p.Asn4549=
ENST00000616098.4:c.13644_13645delinsAC	ENSP00000477990.1:n.13644_13645delinsAC
NM_000384.2:c.13646_13647delinsAC	NP_000375.2:p.Asn4549=
XM_011532809.1:c.5870-2503_5870-2502delinsAC	XP_011531111.1:n.5870-2503_5870-2502delinsAC
NM_000384.3:c.13646_13647delinsAC MANE Select	NP_000375.3:p.Asn4549=