Canonical Allele Identifier: CA2508627066

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023550_21023551insTTCAG , CM000664.2:g.21023550_21023551insTTCAG	GRCh38
NC_000002.11:g.21246422_21246423insTTCAG , CM000664.1:g.21246422_21246423insTTCAG	GRCh37
NC_000002.10:g.21099927_21099928insTTCAG	NCBI36
NG_011793.1:g.25526_25527insAACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1887_*1888insAACTG	ENSP00000501110.2:n.*1887_*1888insAACTG
ENST00000673882.2:c.*1887_*1888insAACTG	ENSP00000501253.2:n.*1887_*1888insAACTG
ENST00000673739.1:c.2295_2296insAACTG	ENSP00000501110.1:n.2295_2296insAACTG
ENST00000673882.1:c.2295_2296insAACTG	ENSP00000501253.1:n.2295_2296insAACTG
ENST00000233242.5:c.2581_2582insAACTG MANE Select	ENSP00000233242.1:p.Gly861GlufsTer4
ENST00000616098.4:c.2581_2582insAACTG	ENSP00000477990.1:p.Gly861GlufsTer4
NM_000384.2:c.2581_2582insAACTG	NP_000375.2:p.Gly861GlufsTer4
XM_011532809.1:c.2581_2582insAACTG	XP_011531111.1:p.Gly861GlufsTer4
NM_000384.3:c.2581_2582insAACTG MANE Select	NP_000375.3:p.Gly861GlufsTer4