Canonical Allele Identifier: CA2515385115
Gene: APOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21021143del , CM000664.2:g.21021143del GRCh38
NC_000002.11:g.21244015del , CM000664.1:g.21244015del GRCh37
NC_000002.10:g.21097520del NCBI36
NG_011793.1:g.27931del

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*2123-1238del ENSP00000501110.2:n.*2123-1238del
ENST00000673882.2:c.*2123-1238del ENSP00000501253.2:n.*2123-1238del
ENST00000673739.1:c.2531-1238del ENSP00000501110.1:n.2531-1238del
ENST00000673882.1:c.2531-1238del ENSP00000501253.1:n.2531-1238del
ENST00000233242.5:c.2817-1238del MANE Select ENSP00000233242.1:n.2817-1238del
ENST00000616098.4:c.2817-1238del ENSP00000477990.1:n.2817-1238del
NM_000384.2:c.2817-1238del NP_000375.2:n.2817-1238del
XM_011532809.1:c.2817-1238del XP_011531111.1:n.2817-1238del
NM_000384.3:c.2817-1238del MANE Select NP_000375.3:n.2817-1238del
Search 100 bp 5'
Search 100 bp 3'