Canonical Allele Identifier: CA697009629
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1205401256
gnomAD v3: 13-27924794-TGGCA-T
gnomAD v4: 13-27924794-TGGCA-T
MyVariant Identifiers: chr13:g.28498932_28498935del (hg19) chr13:g.27924795_27924798del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924796_27924799del , CM000675.2:g.27924796_27924799del GRCh38
NC_000013.10:g.28498933_28498936del , CM000675.1:g.28498933_28498936del GRCh37
NC_000013.9:g.27396933_27396936del NCBI36
NG_008183.1:g.9766_9769del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*95_*98del MANE Select ENSP00000370421.4:n.*95_*98del
ENST00000381033.4:c.*95_*98del ENSP00000370421.4:n.*95_*98del
NM_000209.3:c.*95_*98del NP_000200.1:n.*95_*98del
NM_000209.4:c.*95_*98del MANE Select NP_000200.1:n.*95_*98del
Search 100 bp 5'
Search 100 bp 3'