Canonical Allele Identifier: CA2658048743
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21037905_21037909del , CM000664.2:g.21037905_21037909del GRCh38
NC_000002.11:g.21260777_21260781del , CM000664.1:g.21260777_21260781del GRCh37
NC_000002.10:g.21114282_21114286del NCBI36
NG_011793.1:g.11166_11170del

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.384-653_384-649del ENSP00000501110.2:n.384-653_384-649del
ENST00000673882.2:c.384-653_384-649del ENSP00000501253.2:n.384-653_384-649del
ENST00000673739.1:c.252-653_252-649del ENSP00000501110.1:n.252-653_252-649del
ENST00000673882.1:c.252-653_252-649del ENSP00000501253.1:n.252-653_252-649del
ENST00000233242.5:c.537+50_537+54del MANE Select ENSP00000233242.1:n.537+50_537+54del
ENST00000399256.4:c.537+50_537+54del ENSP00000382200.4:n.537+50_537+54del
ENST00000616098.4:c.537+50_537+54del ENSP00000477990.1:n.537+50_537+54del
NM_000384.2:c.537+50_537+54del NP_000375.2:n.537+50_537+54del
XM_011532809.1:c.537+50_537+54del XP_011531111.1:n.537+50_537+54del
NM_000384.3:c.537+50_537+54del MANE Select NP_000375.3:n.537+50_537+54del