Canonical Allele Identifier: CA2493481631

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21021082_21021083delinsAG , CM000664.2:g.21021082_21021083delinsAG	GRCh38
NC_000002.11:g.21243954_21243955delinsAG , CM000664.1:g.21243954_21243955delinsAG	GRCh37
NC_000002.10:g.21097459_21097460delinsAG	NCBI36
NG_011793.1:g.27991_27992delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2123-1178_*2123-1177delinsCT	ENSP00000501110.2:n.*2123-1178_*2123-1177delinsCT
ENST00000673882.2:c.*2123-1178_*2123-1177delinsCT	ENSP00000501253.2:n.*2123-1178_*2123-1177delinsCT
ENST00000673739.1:c.2531-1178_2531-1177delinsCT	ENSP00000501110.1:n.2531-1178_2531-1177delinsCT
ENST00000673882.1:c.2531-1178_2531-1177delinsCT	ENSP00000501253.1:n.2531-1178_2531-1177delinsCT
ENST00000233242.5:c.2817-1178_2817-1177delinsCT MANE Select	ENSP00000233242.1:n.2817-1178_2817-1177delinsCT
ENST00000616098.4:c.2817-1178_2817-1177delinsCT	ENSP00000477990.1:n.2817-1178_2817-1177delinsCT
NM_000384.2:c.2817-1178_2817-1177delinsCT	NP_000375.2:n.2817-1178_2817-1177delinsCT
XM_011532809.1:c.2817-1178_2817-1177delinsCT	XP_011531111.1:n.2817-1178_2817-1177delinsCT
NM_000384.3:c.2817-1178_2817-1177delinsCT MANE Select	NP_000375.3:n.2817-1178_2817-1177delinsCT