Canonical Allele Identifier: CA2658057176
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21015443-T-TCCA
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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
Search 100 bp 5'
Search 100 bp 3'