Canonical Allele Identifier: CA2493482673

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023418_21023419delinsAG , CM000664.2:g.21023418_21023419delinsAG	GRCh38
NC_000002.11:g.21246290_21246291delinsAG , CM000664.1:g.21246290_21246291delinsAG	GRCh37
NC_000002.10:g.21099795_21099796delinsAG	NCBI36
NG_011793.1:g.25655_25656delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1910+106_*1910+107delinsCT	ENSP00000501110.2:n.*1910+106_*1910+107delinsCT
ENST00000673882.2:c.*1910+106_*1910+107delinsCT	ENSP00000501253.2:n.*1910+106_*1910+107delinsCT
ENST00000673739.1:c.2318+106_2318+107delinsCT	ENSP00000501110.1:n.2318+106_2318+107delinsCT
ENST00000673882.1:c.2318+106_2318+107delinsCT	ENSP00000501253.1:n.2318+106_2318+107delinsCT
ENST00000233242.5:c.2604+106_2604+107delinsCT MANE Select	ENSP00000233242.1:n.2604+106_2604+107delinsCT
ENST00000616098.4:c.2604+106_2604+107delinsCT	ENSP00000477990.1:n.2604+106_2604+107delinsCT
NM_000384.2:c.2604+106_2604+107delinsCT	NP_000375.2:n.2604+106_2604+107delinsCT
XM_011532809.1:c.2604+106_2604+107delinsCT	XP_011531111.1:n.2604+106_2604+107delinsCT
NM_000384.3:c.2604+106_2604+107delinsCT MANE Select	NP_000375.3:n.2604+106_2604+107delinsCT