Canonical Allele Identifier: CA645517011

Gene: APOB

Linked Data

• COSMIC: COSM6008865

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015507del , CM000664.2:g.21015507del	GRCh38
NC_000002.11:g.21238379del , CM000664.1:g.21238379del	GRCh37
NC_000002.10:g.21091884del	NCBI36
NG_011793.1:g.33569del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2679del	ENSP00000501110.2:n.*2679del
ENST00000673882.2:c.*2468del	ENSP00000501253.2:n.*2468del
ENST00000673739.1:c.3087del	ENSP00000501110.1:n.3087del
ENST00000673882.1:c.2876del	ENSP00000501253.1:n.2876del
ENST00000233242.5:c.3373del MANE Select	ENSP00000233242.1:p.Ser1125ProfsTer?
ENST00000616098.4:c.3373del	ENSP00000477990.1:p.Ser1125ProfsTer?
NM_000384.2:c.3373del	NP_000375.2:p.Ser1125ProfsTer?
XM_011532809.1:c.3373del	XP_011531111.1:p.Ser1125ProfsTer?
NM_000384.3:c.3373del MANE Select	NP_000375.3:p.Ser1125ProfsTer?