Canonical Allele Identifier: CA2749100374

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21043833_21043836del , CM000664.2:g.21043833_21043836del	GRCh38
NC_000002.11:g.21266705_21266708del , CM000664.1:g.21266705_21266708del	GRCh37
NC_000002.10:g.21120210_21120213del	NCBI36
NG_011793.1:g.5238_5241del

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.82+28_82+31del	ENSP00000501110.2:n.82+28_82+31del
ENST00000673882.2:c.82+28_82+31del	ENSP00000501253.2:n.82+28_82+31del
ENST00000233242.5:c.82+28_82+31del MANE Select	ENSP00000233242.1:n.82+28_82+31del
ENST00000399256.4:c.82+28_82+31del	ENSP00000382200.4:n.82+28_82+31del
ENST00000616098.4:c.82+28_82+31del	ENSP00000477990.1:n.82+28_82+31del
NM_000384.2:c.82+28_82+31del	NP_000375.2:n.82+28_82+31del
XM_011532809.1:c.82+28_82+31del	XP_011531111.1:n.82+28_82+31del
NM_000384.3:c.82+28_82+31del MANE Select	NP_000375.3:n.82+28_82+31del