Canonical Allele Identifier: CA2658057176

Gene: APOB

Linked Data

• gnomAD v4: 2-21015443-T-TCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015443_21015444insCCA , CM000664.2:g.21015443_21015444insCCA	GRCh38
NC_000002.11:g.21238315_21238316insCCA , CM000664.1:g.21238315_21238316insCCA	GRCh37
NC_000002.10:g.21091820_21091821insCCA	NCBI36
NG_011793.1:g.33630_33631insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2740_*2741insTGG	ENSP00000501110.2:n.*2740_*2741insTGG
ENST00000673882.2:c.*2529_*2530insTGG	ENSP00000501253.2:n.*2529_*2530insTGG
ENST00000673739.1:c.3148_3149insTGG	ENSP00000501110.1:n.3148_3149insTGG
ENST00000673882.1:c.2937_2938insTGG	ENSP00000501253.1:n.2937_2938insTGG
ENST00000233242.5:c.3434_3435insTGG MANE Select	ENSP00000233242.1:p.Lys1145delinsAsnGly
ENST00000616098.4:c.3434_3435insTGG	ENSP00000477990.1:p.Lys1145delinsAsnGly
NM_000384.2:c.3434_3435insTGG	NP_000375.2:p.Lys1145delinsAsnGly
XM_011532809.1:c.3434_3435insTGG	XP_011531111.1:p.Lys1145delinsAsnGly
NM_000384.3:c.3434_3435insTGG MANE Select	NP_000375.3:p.Lys1145delinsAsnGly