Canonical Allele Identifier: CA2493481635

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21021087_21021088delinsTA , CM000664.2:g.21021087_21021088delinsTA	GRCh38
NC_000002.11:g.21243959_21243960delinsTA , CM000664.1:g.21243959_21243960delinsTA	GRCh37
NC_000002.10:g.21097464_21097465delinsTA	NCBI36
NG_011793.1:g.27986_27987delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2123-1183_*2123-1182delinsTA	ENSP00000501110.2:n.*2123-1183_*2123-1182delinsTA
ENST00000673882.2:c.*2123-1183_*2123-1182delinsTA	ENSP00000501253.2:n.*2123-1183_*2123-1182delinsTA
ENST00000673739.1:c.2531-1183_2531-1182delinsTA	ENSP00000501110.1:n.2531-1183_2531-1182delinsTA
ENST00000673882.1:c.2531-1183_2531-1182delinsTA	ENSP00000501253.1:n.2531-1183_2531-1182delinsTA
ENST00000233242.5:c.2817-1183_2817-1182delinsTA MANE Select	ENSP00000233242.1:n.2817-1183_2817-1182delinsTA
ENST00000616098.4:c.2817-1183_2817-1182delinsTA	ENSP00000477990.1:n.2817-1183_2817-1182delinsTA
NM_000384.2:c.2817-1183_2817-1182delinsTA	NP_000375.2:n.2817-1183_2817-1182delinsTA
XM_011532809.1:c.2817-1183_2817-1182delinsTA	XP_011531111.1:n.2817-1183_2817-1182delinsTA
NM_000384.3:c.2817-1183_2817-1182delinsTA MANE Select	NP_000375.3:n.2817-1183_2817-1182delinsTA