Canonical Allele Identifier: CA2493482661

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023387_21023388delinsTA , CM000664.2:g.21023387_21023388delinsTA	GRCh38
NC_000002.11:g.21246259_21246260delinsTA , CM000664.1:g.21246259_21246260delinsTA	GRCh37
NC_000002.10:g.21099764_21099765delinsTA	NCBI36
NG_011793.1:g.25686_25687delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1910+137_*1910+138delinsTA	ENSP00000501110.2:n.*1910+137_*1910+138delinsTA
ENST00000673882.2:c.*1910+137_*1910+138delinsTA	ENSP00000501253.2:n.*1910+137_*1910+138delinsTA
ENST00000673739.1:c.2318+137_2318+138delinsTA	ENSP00000501110.1:n.2318+137_2318+138delinsTA
ENST00000673882.1:c.2318+137_2318+138delinsTA	ENSP00000501253.1:n.2318+137_2318+138delinsTA
ENST00000233242.5:c.2604+137_2604+138delinsTA MANE Select	ENSP00000233242.1:n.2604+137_2604+138delinsTA
ENST00000616098.4:c.2604+137_2604+138delinsTA	ENSP00000477990.1:n.2604+137_2604+138delinsTA
NM_000384.2:c.2604+137_2604+138delinsTA	NP_000375.2:n.2604+137_2604+138delinsTA
XM_011532809.1:c.2604+137_2604+138delinsTA	XP_011531111.1:n.2604+137_2604+138delinsTA
NM_000384.3:c.2604+137_2604+138delinsTA MANE Select	NP_000375.3:n.2604+137_2604+138delinsTA