Canonical Allele Identifier: CA2493489509

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038406_21038407delinsAG , CM000664.2:g.21038406_21038407delinsAG	GRCh38
NC_000002.11:g.21261278_21261279delinsAG , CM000664.1:g.21261278_21261279delinsAG	GRCh37
NC_000002.10:g.21114783_21114784delinsAG	NCBI36
NG_011793.1:g.10667_10668delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1152_384-1151delinsCT	ENSP00000501110.2:n.384-1152_384-1151delinsCT
ENST00000673882.2:c.384-1152_384-1151delinsCT	ENSP00000501253.2:n.384-1152_384-1151delinsCT
ENST00000673739.1:c.252-1152_252-1151delinsCT	ENSP00000501110.1:n.252-1152_252-1151delinsCT
ENST00000673882.1:c.252-1152_252-1151delinsCT	ENSP00000501253.1:n.252-1152_252-1151delinsCT
ENST00000233242.5:c.384-296_384-295delinsCT MANE Select	ENSP00000233242.1:n.384-296_384-295delinsCT
ENST00000399256.4:c.384-296_384-295delinsCT	ENSP00000382200.4:n.384-296_384-295delinsCT
ENST00000616098.4:c.384-296_384-295delinsCT	ENSP00000477990.1:n.384-296_384-295delinsCT
NM_000384.2:c.384-296_384-295delinsCT	NP_000375.2:n.384-296_384-295delinsCT
XM_011532809.1:c.384-296_384-295delinsCT	XP_011531111.1:n.384-296_384-295delinsCT
NM_000384.3:c.384-296_384-295delinsCT MANE Select	NP_000375.3:n.384-296_384-295delinsCT