Canonical Allele Identifier: CA2493472558

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21001664_21001665delinsAT , CM000664.2:g.21001664_21001665delinsAT	GRCh38
NC_000002.11:g.21224536_21224537delinsAT , CM000664.1:g.21224536_21224537delinsAT	GRCh37
NC_000002.10:g.21078041_21078042delinsAT	NCBI36
NG_011793.1:g.47409_47410delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.*65_*66delinsAT MANE Select	ENSP00000233242.1:n.*65_*66delinsAT
ENST00000616098.4:c.13755_13756delinsAT	ENSP00000477990.1:n.13755_13756delinsAT
NM_000384.2:c.*65_*66delinsAT	NP_000375.2:n.*65_*66delinsAT
XM_011532809.1:c.5870-2392_5870-2391delinsAT	XP_011531111.1:n.5870-2392_5870-2391delinsAT
NM_000384.3:c.*65_*66delinsAT MANE Select	NP_000375.3:n.*65_*66delinsAT