Canonical Allele Identifier: CA2493481685
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21021190_21021191delinsCA , CM000664.2:g.21021190_21021191delinsCA GRCh38
NC_000002.11:g.21244062_21244063delinsCA , CM000664.1:g.21244062_21244063delinsCA GRCh37
NC_000002.10:g.21097567_21097568delinsCA NCBI36
NG_011793.1:g.27883_27884delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2123-1286_*2123-1285delinsTG ENSP00000501110.2:n.*2123-1286_*2123-1285delinsTG
ENST00000673882.2:c.*2123-1286_*2123-1285delinsTG ENSP00000501253.2:n.*2123-1286_*2123-1285delinsTG
ENST00000673739.1:c.2531-1286_2531-1285delinsTG ENSP00000501110.1:n.2531-1286_2531-1285delinsTG
ENST00000673882.1:c.2531-1286_2531-1285delinsTG ENSP00000501253.1:n.2531-1286_2531-1285delinsTG
ENST00000233242.5:c.2817-1286_2817-1285delinsTG MANE Select ENSP00000233242.1:n.2817-1286_2817-1285delinsTG
ENST00000616098.4:c.2817-1286_2817-1285delinsTG ENSP00000477990.1:n.2817-1286_2817-1285delinsTG
NM_000384.2:c.2817-1286_2817-1285delinsTG NP_000375.2:n.2817-1286_2817-1285delinsTG
XM_011532809.1:c.2817-1286_2817-1285delinsTG XP_011531111.1:n.2817-1286_2817-1285delinsTG
NM_000384.3:c.2817-1286_2817-1285delinsTG MANE Select NP_000375.3:n.2817-1286_2817-1285delinsTG