Canonical Allele Identifier: CA2658057080

Gene: APOB

Linked Data

• gnomAD v4: 2-21015295-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015296del , CM000664.2:g.21015296del	GRCh38
NC_000002.11:g.21238168del , CM000664.1:g.21238168del	GRCh37
NC_000002.10:g.21091673del	NCBI36
NG_011793.1:g.33778del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2815-36del	ENSP00000501110.2:n.*2815-36del
ENST00000673882.2:c.*2604-36del	ENSP00000501253.2:n.*2604-36del
ENST00000673739.1:c.3223-36del	ENSP00000501110.1:n.3223-36del
ENST00000673882.1:c.3012-36del	ENSP00000501253.1:n.3012-36del
ENST00000233242.5:c.3509-36del MANE Select	ENSP00000233242.1:n.3509-36del
ENST00000616098.4:c.3509-36del	ENSP00000477990.1:n.3509-36del
NM_000384.2:c.3509-36del	NP_000375.2:n.3509-36del
XM_011532809.1:c.3509-36del	XP_011531111.1:n.3509-36del
NM_000384.3:c.3509-36del MANE Select	NP_000375.3:n.3509-36del