Canonical Allele Identifier: CA2493482717

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023514_21023515delinsCA , CM000664.2:g.21023514_21023515delinsCA	GRCh38
NC_000002.11:g.21246386_21246387delinsCA , CM000664.1:g.21246386_21246387delinsCA	GRCh37
NC_000002.10:g.21099891_21099892delinsCA	NCBI36
NG_011793.1:g.25559_25560delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1910+10_*1910+11delinsTG	ENSP00000501110.2:n.*1910+10_*1910+11delinsTG
ENST00000673882.2:c.*1910+10_*1910+11delinsTG	ENSP00000501253.2:n.*1910+10_*1910+11delinsTG
ENST00000673739.1:c.2318+10_2318+11delinsTG	ENSP00000501110.1:n.2318+10_2318+11delinsTG
ENST00000673882.1:c.2318+10_2318+11delinsTG	ENSP00000501253.1:n.2318+10_2318+11delinsTG
ENST00000233242.5:c.2604+10_2604+11delinsTG MANE Select	ENSP00000233242.1:n.2604+10_2604+11delinsTG
ENST00000616098.4:c.2604+10_2604+11delinsTG	ENSP00000477990.1:n.2604+10_2604+11delinsTG
NM_000384.2:c.2604+10_2604+11delinsTG	NP_000375.2:n.2604+10_2604+11delinsTG
XM_011532809.1:c.2604+10_2604+11delinsTG	XP_011531111.1:n.2604+10_2604+11delinsTG
NM_000384.3:c.2604+10_2604+11delinsTG MANE Select	NP_000375.3:n.2604+10_2604+11delinsTG