Canonical Allele Identifier: CA2576687097

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037933_21037934insTGAA , CM000664.2:g.21037933_21037934insTGAA	GRCh38
NC_000002.11:g.21260805_21260806insTGAA , CM000664.1:g.21260805_21260806insTGAA	GRCh37
NC_000002.10:g.21114310_21114311insTGAA	NCBI36
NG_011793.1:g.11140_11141insTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-679_384-678insTTCA	ENSP00000501110.2:n.384-679_384-678insTTCA
ENST00000673882.2:c.384-679_384-678insTTCA	ENSP00000501253.2:n.384-679_384-678insTTCA
ENST00000673739.1:c.252-679_252-678insTTCA	ENSP00000501110.1:n.252-679_252-678insTTCA
ENST00000673882.1:c.252-679_252-678insTTCA	ENSP00000501253.1:n.252-679_252-678insTTCA
ENST00000233242.5:c.537+24_537+25insTTCA MANE Select	ENSP00000233242.1:n.537+24_537+25insTTCA
ENST00000399256.4:c.537+24_537+25insTTCA	ENSP00000382200.4:n.537+24_537+25insTTCA
ENST00000616098.4:c.537+24_537+25insTTCA	ENSP00000477990.1:n.537+24_537+25insTTCA
NM_000384.2:c.537+24_537+25insTTCA	NP_000375.2:n.537+24_537+25insTTCA
XM_011532809.1:c.537+24_537+25insTTCA	XP_011531111.1:n.537+24_537+25insTTCA
NM_000384.3:c.537+24_537+25insTTCA MANE Select	NP_000375.3:n.537+24_537+25insTTCA