Canonical Allele Identifier: CA387643838
Gene: PDX1 HGNC NCBI
PLUT HGNC NCBI

Linked Data

dbSNP Id: rs1340060753
gnomAD v2: 13-28494369-C-T
gnomAD v4: 13-27920232-C-T
MyVariant Identifiers: chr13:g.28494369C>T (hg19) chr13:g.27920232C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920232C>T , CM000675.2:g.27920232C>T GRCh38
NC_000013.10:g.28494369C>T , CM000675.1:g.28494369C>T GRCh37
NC_000013.9:g.27392369C>T NCBI36
NG_008183.1:g.5202C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.94C>T (PDX1) MANE Select ENSP00000370421.4:p.Pro32Ser
ENST00000381033.4:c.94C>T (PDX1) ENSP00000370421.4:p.Pro32Ser
NM_000209.3:c.94C>T (PDX1) NP_000200.1:p.Pro32Ser
NR_047484.1:n.241+932G>A (PLUT)
XR_941578.1:n.239C>T (PDX1)
XR_941579.1:n.239C>T (PDX1)
XR_941580.1:n.239C>T (PDX1)
XR_941578.2:n.251C>T (PDX1)
XR_941580.2:n.251C>T (PDX1)
NM_000209.4:c.94C>T (PDX1) MANE Select NP_000200.1:p.Pro32Ser
Search 100 bp 5'
Search 100 bp 3'