Canonical Allele Identifier: CA2658056827

Gene: APOB

Linked Data

• gnomAD v4: 2-21014955-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014960_21014961del , CM000664.2:g.21014960_21014961del	GRCh38
NC_000002.11:g.21237832_21237833del , CM000664.1:g.21237832_21237833del	GRCh37
NC_000002.10:g.21091337_21091338del	NCBI36
NG_011793.1:g.34117_34118del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+116_*3002+117del	ENSP00000501110.2:n.*3002+116_*3002+117del
ENST00000673882.2:c.*2791+116_*2791+117del	ENSP00000501253.2:n.*2791+116_*2791+117del
ENST00000673739.1:c.3410+116_3410+117del	ENSP00000501110.1:n.3410+116_3410+117del
ENST00000673882.1:c.3199+116_3199+117del	ENSP00000501253.1:n.3199+116_3199+117del
ENST00000233242.5:c.3696+116_3696+117del MANE Select	ENSP00000233242.1:n.3696+116_3696+117del
ENST00000616098.4:c.3696+116_3696+117del	ENSP00000477990.1:n.3696+116_3696+117del
NM_000384.2:c.3696+116_3696+117del	NP_000375.2:n.3696+116_3696+117del
XM_011532809.1:c.3696+116_3696+117del	XP_011531111.1:n.3696+116_3696+117del
NM_000384.3:c.3696+116_3696+117del MANE Select	NP_000375.3:n.3696+116_3696+117del