Canonical Allele Identifier: CA2493478808

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014955_21014956delinsTG , CM000664.2:g.21014955_21014956delinsTG	GRCh38
NC_000002.11:g.21237827_21237828delinsTG , CM000664.1:g.21237827_21237828delinsTG	GRCh37
NC_000002.10:g.21091332_21091333delinsTG	NCBI36
NG_011793.1:g.34118_34119delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+117_*3002+118delinsCA	ENSP00000501110.2:n.*3002+117_*3002+118delinsCA
ENST00000673882.2:c.*2791+117_*2791+118delinsCA	ENSP00000501253.2:n.*2791+117_*2791+118delinsCA
ENST00000673739.1:c.3410+117_3410+118delinsCA	ENSP00000501110.1:n.3410+117_3410+118delinsCA
ENST00000673882.1:c.3199+117_3199+118delinsCA	ENSP00000501253.1:n.3199+117_3199+118delinsCA
ENST00000233242.5:c.3696+117_3696+118delinsCA MANE Select	ENSP00000233242.1:n.3696+117_3696+118delinsCA
ENST00000616098.4:c.3696+117_3696+118delinsCA	ENSP00000477990.1:n.3696+117_3696+118delinsCA
NM_000384.2:c.3696+117_3696+118delinsCA	NP_000375.2:n.3696+117_3696+118delinsCA
XM_011532809.1:c.3696+117_3696+118delinsCA	XP_011531111.1:n.3696+117_3696+118delinsCA
NM_000384.3:c.3696+117_3696+118delinsCA MANE Select	NP_000375.3:n.3696+117_3696+118delinsCA