Canonical Allele Identifier: CA2622478644
Gene: PDX1 HGNC NCBI

Linked Data

gnomAD v4: 13-27924829-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924831del , CM000675.2:g.27924831del GRCh38
NC_000013.10:g.28498968del , CM000675.1:g.28498968del GRCh37
NC_000013.9:g.27396968del NCBI36
NG_008183.1:g.9801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*130del MANE Select ENSP00000370421.4:n.*130del
ENST00000381033.4:c.*130del ENSP00000370421.4:n.*130del
NM_000209.3:c.*130del NP_000200.1:n.*130del
NM_000209.4:c.*130del MANE Select NP_000200.1:n.*130del
Search 100 bp 5'
Search 100 bp 3'