Canonical Allele Identifier: CA2493489250

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037908_21037911delinsCATG , CM000664.2:g.21037908_21037911delinsCATG	GRCh38
NC_000002.11:g.21260780_21260783delinsCATG , CM000664.1:g.21260780_21260783delinsCATG	GRCh37
NC_000002.10:g.21114285_21114288delinsCATG	NCBI36
NG_011793.1:g.11163_11166delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-656_384-653delinsCATG	ENSP00000501110.2:n.384-656_384-653delinsCATG
ENST00000673882.2:c.384-656_384-653delinsCATG	ENSP00000501253.2:n.384-656_384-653delinsCATG
ENST00000673739.1:c.252-656_252-653delinsCATG	ENSP00000501110.1:n.252-656_252-653delinsCATG
ENST00000673882.1:c.252-656_252-653delinsCATG	ENSP00000501253.1:n.252-656_252-653delinsCATG
ENST00000233242.5:c.537+47_537+50delinsCATG MANE Select	ENSP00000233242.1:n.537+47_537+50delinsCATG
ENST00000399256.4:c.537+47_537+50delinsCATG	ENSP00000382200.4:n.537+47_537+50delinsCATG
ENST00000616098.4:c.537+47_537+50delinsCATG	ENSP00000477990.1:n.537+47_537+50delinsCATG
NM_000384.2:c.537+47_537+50delinsCATG	NP_000375.2:n.537+47_537+50delinsCATG
XM_011532809.1:c.537+47_537+50delinsCATG	XP_011531111.1:n.537+47_537+50delinsCATG
NM_000384.3:c.537+47_537+50delinsCATG MANE Select	NP_000375.3:n.537+47_537+50delinsCATG