Canonical Allele Identifier: CA645517693

Gene: APOB

Linked Data - Expert Curation

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21041027_21041028delinsAA , CM000664.2:g.21041027_21041028delinsAA	GRCh38
NC_000002.11:g.21263899_21263900delinsAA , CM000664.1:g.21263899_21263900delinsAA	GRCh37
NC_000002.10:g.21117404_21117405delinsAA	NCBI36
NG_011793.1:g.8046_8047delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.293_294delinsTT	ENSP00000501110.2:p.Thr98Ile
ENST00000673882.2:c.293_294delinsTT	ENSP00000501253.2:p.Thr98Ile
ENST00000673739.1:c.161_162delinsTT	ENSP00000501110.1:p.Thr54Ile
ENST00000673882.1:c.161_162delinsTT	ENSP00000501253.1:p.Thr54Ile
ENST00000233242.5:c.293_294delinsTT MANE Select	ENSP00000233242.1:p.Thr98Ile
ENST00000399256.4:c.293_294delinsTT	ENSP00000382200.4:p.Thr98Ile
ENST00000616098.4:c.293_294delinsTT	ENSP00000477990.1:p.Thr98Ile
NM_000384.2:c.293_294delinsTT	NP_000375.2:p.Thr98Ile
XM_011532809.1:c.293_294delinsTT	XP_011531111.1:p.Thr98Ile
NM_000384.3:c.293_294delinsTT MANE Select	NP_000375.3:p.Thr98Ile