Canonical Allele Identifier: CA2493489448

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038316_21038320delinsCTTTT , CM000664.2:g.21038316_21038320delinsCTTTT	GRCh38
NC_000002.11:g.21261188_21261192delinsCTTTT , CM000664.1:g.21261188_21261192delinsCTTTT	GRCh37
NC_000002.10:g.21114693_21114697delinsCTTTT	NCBI36
NG_011793.1:g.10754_10758delinsAAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1065_384-1061delinsAAAAG	ENSP00000501110.2:n.384-1065_384-1061delinsAAAAG
ENST00000673882.2:c.384-1065_384-1061delinsAAAAG	ENSP00000501253.2:n.384-1065_384-1061delinsAAAAG
ENST00000673739.1:c.252-1065_252-1061delinsAAAAG	ENSP00000501110.1:n.252-1065_252-1061delinsAAAAG
ENST00000673882.1:c.252-1065_252-1061delinsAAAAG	ENSP00000501253.1:n.252-1065_252-1061delinsAAAAG
ENST00000233242.5:c.384-209_384-205delinsAAAAG MANE Select	ENSP00000233242.1:n.384-209_384-205delinsAAAAG
ENST00000399256.4:c.384-209_384-205delinsAAAAG	ENSP00000382200.4:n.384-209_384-205delinsAAAAG
ENST00000616098.4:c.384-209_384-205delinsAAAAG	ENSP00000477990.1:n.384-209_384-205delinsAAAAG
NM_000384.2:c.384-209_384-205delinsAAAAG	NP_000375.2:n.384-209_384-205delinsAAAAG
XM_011532809.1:c.384-209_384-205delinsAAAAG	XP_011531111.1:n.384-209_384-205delinsAAAAG
NM_000384.3:c.384-209_384-205delinsAAAAG MANE Select	NP_000375.3:n.384-209_384-205delinsAAAAG