Canonical Allele Identifier: CA2493479036

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015444T= , CM000664.2:g.21015444T=	GRCh38
NC_000002.11:g.21238316T= , CM000664.1:g.21238316T=	GRCh37
NC_000002.10:g.21091821T=	NCBI36
NG_011793.1:g.33630A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2740A=	ENSP00000501110.2:n.*2740A=
ENST00000673882.2:c.*2529A=	ENSP00000501253.2:n.*2529A=
ENST00000673739.1:c.3148A=	ENSP00000501110.1:n.3148A=
ENST00000673882.1:c.2937A=	ENSP00000501253.1:n.2937A=
ENST00000233242.5:c.3434A= MANE Select	ENSP00000233242.1:p.Lys1145=
ENST00000616098.4:c.3434A=	ENSP00000477990.1:p.Lys1145=
NM_000384.2:c.3434A=	NP_000375.2:p.Lys1145=
XM_011532809.1:c.3434A=	XP_011531111.1:p.Lys1145=
NM_000384.3:c.3434A= MANE Select	NP_000375.3:p.Lys1145=