Canonical Allele Identifier: CA2493482703

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023482_21023483delinsGA , CM000664.2:g.21023482_21023483delinsGA	GRCh38
NC_000002.11:g.21246354_21246355delinsGA , CM000664.1:g.21246354_21246355delinsGA	GRCh37
NC_000002.10:g.21099859_21099860delinsGA	NCBI36
NG_011793.1:g.25591_25592delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1910+42_*1910+43delinsTC	ENSP00000501110.2:n.*1910+42_*1910+43delinsTC
ENST00000673882.2:c.*1910+42_*1910+43delinsTC	ENSP00000501253.2:n.*1910+42_*1910+43delinsTC
ENST00000673739.1:c.2318+42_2318+43delinsTC	ENSP00000501110.1:n.2318+42_2318+43delinsTC
ENST00000673882.1:c.2318+42_2318+43delinsTC	ENSP00000501253.1:n.2318+42_2318+43delinsTC
ENST00000233242.5:c.2604+42_2604+43delinsTC MANE Select	ENSP00000233242.1:n.2604+42_2604+43delinsTC
ENST00000616098.4:c.2604+42_2604+43delinsTC	ENSP00000477990.1:n.2604+42_2604+43delinsTC
NM_000384.2:c.2604+42_2604+43delinsTC	NP_000375.2:n.2604+42_2604+43delinsTC
XM_011532809.1:c.2604+42_2604+43delinsTC	XP_011531111.1:n.2604+42_2604+43delinsTC
NM_000384.3:c.2604+42_2604+43delinsTC MANE Select	NP_000375.3:n.2604+42_2604+43delinsTC