Canonical Allele Identifier: CA2493479001

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015351_21015353delinsCAG , CM000664.2:g.21015351_21015353delinsCAG	GRCh38
NC_000002.11:g.21238223_21238225delinsCAG , CM000664.1:g.21238223_21238225delinsCAG	GRCh37
NC_000002.10:g.21091728_21091730delinsCAG	NCBI36
NG_011793.1:g.33721_33723delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2814+17_*2814+19delinsCTG	ENSP00000501110.2:n.*2814+17_*2814+19delinsCTG
ENST00000673882.2:c.*2603+17_*2603+19delinsCTG	ENSP00000501253.2:n.*2603+17_*2603+19delinsCTG
ENST00000673739.1:c.3222+17_3222+19delinsCTG	ENSP00000501110.1:n.3222+17_3222+19delinsCTG
ENST00000673882.1:c.3011+17_3011+19delinsCTG	ENSP00000501253.1:n.3011+17_3011+19delinsCTG
ENST00000233242.5:c.3508+17_3508+19delinsCTG MANE Select	ENSP00000233242.1:n.3508+17_3508+19delinsCTG
ENST00000616098.4:c.3508+17_3508+19delinsCTG	ENSP00000477990.1:n.3508+17_3508+19delinsCTG
NM_000384.2:c.3508+17_3508+19delinsCTG	NP_000375.2:n.3508+17_3508+19delinsCTG
XM_011532809.1:c.3508+17_3508+19delinsCTG	XP_011531111.1:n.3508+17_3508+19delinsCTG
NM_000384.3:c.3508+17_3508+19delinsCTG MANE Select	NP_000375.3:n.3508+17_3508+19delinsCTG