Canonical Allele Identifier: CA2658057174

Gene: APOB

Linked Data

• gnomAD v4: 2-21015440-C-CTGTAGCAGATG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015440_21015441insTGTAGCAGATG , CM000664.2:g.21015440_21015441insTGTAGCAGATG	GRCh38
NC_000002.11:g.21238312_21238313insTGTAGCAGATG , CM000664.1:g.21238312_21238313insTGTAGCAGATG	GRCh37
NC_000002.10:g.21091817_21091818insTGTAGCAGATG	NCBI36
NG_011793.1:g.33633_33634insCATCTGCTACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2743_*2744insCATCTGCTACA	ENSP00000501110.2:n.*2743_*2744insCATCTGCTACA
ENST00000673882.2:c.*2532_*2533insCATCTGCTACA	ENSP00000501253.2:n.*2532_*2533insCATCTGCTACA
ENST00000673739.1:c.3151_3152insCATCTGCTACA	ENSP00000501110.1:n.3151_3152insCATCTGCTACA
ENST00000673882.1:c.2940_2941insCATCTGCTACA	ENSP00000501253.1:n.2940_2941insCATCTGCTACA
ENST00000233242.5:c.3437_3438insCATCTGCTACA MANE Select	ENSP00000233242.1:p.Leu1147IlefsTer?
ENST00000616098.4:c.3437_3438insCATCTGCTACA	ENSP00000477990.1:p.Leu1147IlefsTer?
NM_000384.2:c.3437_3438insCATCTGCTACA	NP_000375.2:p.Leu1147IlefsTer?
XM_011532809.1:c.3437_3438insCATCTGCTACA	XP_011531111.1:p.Leu1147IlefsTer?
NM_000384.3:c.3437_3438insCATCTGCTACA MANE Select	NP_000375.3:p.Leu1147IlefsTer?