Canonical Allele Identifier: CA2545747267

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038322_21038323insGAAAATGTA , CM000664.2:g.21038322_21038323insGAAAATGTA	GRCh38
NC_000002.11:g.21261194_21261195insGAAAATGTA , CM000664.1:g.21261194_21261195insGAAAATGTA	GRCh37
NC_000002.10:g.21114699_21114700insGAAAATGTA	NCBI36
NG_011793.1:g.10751_10752insTACATTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1068_384-1067insTACATTTTC	ENSP00000501110.2:n.384-1068_384-1067insTACATTTTC
ENST00000673882.2:c.384-1068_384-1067insTACATTTTC	ENSP00000501253.2:n.384-1068_384-1067insTACATTTTC
ENST00000673739.1:c.252-1068_252-1067insTACATTTTC	ENSP00000501110.1:n.252-1068_252-1067insTACATTTTC
ENST00000673882.1:c.252-1068_252-1067insTACATTTTC	ENSP00000501253.1:n.252-1068_252-1067insTACATTTTC
ENST00000233242.5:c.384-212_384-211insTACATTTTC MANE Select	ENSP00000233242.1:n.384-212_384-211insTACATTTTC
ENST00000399256.4:c.384-212_384-211insTACATTTTC	ENSP00000382200.4:n.384-212_384-211insTACATTTTC
ENST00000616098.4:c.384-212_384-211insTACATTTTC	ENSP00000477990.1:n.384-212_384-211insTACATTTTC
NM_000384.2:c.384-212_384-211insTACATTTTC	NP_000375.2:n.384-212_384-211insTACATTTTC
XM_011532809.1:c.384-212_384-211insTACATTTTC	XP_011531111.1:n.384-212_384-211insTACATTTTC
NM_000384.3:c.384-212_384-211insTACATTTTC MANE Select	NP_000375.3:n.384-212_384-211insTACATTTTC