Canonical Allele Identifier: CA608741264
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1209180442
gnomAD v2: 13-28498869-TC-T
gnomAD v4: 13-27924732-TC-T
MyVariant Identifiers: chr13:g.28498870del (hg19) chr13:g.27924733del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924733del , CM000675.2:g.27924733del GRCh38
NC_000013.10:g.28498870del , CM000675.1:g.28498870del GRCh37
NC_000013.9:g.27396870del NCBI36
NG_008183.1:g.9703del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*32del MANE Select ENSP00000370421.4:n.*32del
ENST00000381033.4:c.*32del ENSP00000370421.4:n.*32del
NM_000209.3:c.*32del NP_000200.1:n.*32del
NM_000209.4:c.*32del MANE Select NP_000200.1:n.*32del
Search 100 bp 5'
Search 100 bp 3'