Canonical Allele Identifier: CA646550581

Gene: APOB

Linked Data

• COSMIC: COSN1822495

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038312_21038315del , CM000664.2:g.21038312_21038315del	GRCh38
NC_000002.11:g.21261184_21261187del , CM000664.1:g.21261184_21261187del	GRCh37
NC_000002.10:g.21114689_21114692del	NCBI36
NG_011793.1:g.10760_10763del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1059_384-1056del	ENSP00000501110.2:n.384-1059_384-1056del
ENST00000673882.2:c.384-1059_384-1056del	ENSP00000501253.2:n.384-1059_384-1056del
ENST00000673739.1:c.252-1059_252-1056del	ENSP00000501110.1:n.252-1059_252-1056del
ENST00000673882.1:c.252-1059_252-1056del	ENSP00000501253.1:n.252-1059_252-1056del
ENST00000233242.5:c.384-203_384-200del MANE Select	ENSP00000233242.1:n.384-203_384-200del
ENST00000399256.4:c.384-203_384-200del	ENSP00000382200.4:n.384-203_384-200del
ENST00000616098.4:c.384-203_384-200del	ENSP00000477990.1:n.384-203_384-200del
NM_000384.2:c.384-203_384-200del	NP_000375.2:n.384-203_384-200del
XM_011532809.1:c.384-203_384-200del	XP_011531111.1:n.384-203_384-200del
NM_000384.3:c.384-203_384-200del MANE Select	NP_000375.3:n.384-203_384-200del