Canonical Allele Identifier: CA387645372
Gene: PDX1 HGNC NCBI

Linked Data

COSMIC: COSM5962708
MyVariant Identifiers: chr13:g.28498450G>A (hg19) chr13:g.27924313G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924313G>A , CM000675.2:g.27924313G>A GRCh38
NC_000013.10:g.28498450G>A , CM000675.1:g.28498450G>A GRCh37
NC_000013.9:g.27396450G>A NCBI36
NG_008183.1:g.9283G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.464G>A MANE Select ENSP00000370421.4:p.Arg155His
ENST00000381033.4:c.464G>A ENSP00000370421.4:p.Arg155His
NM_000209.3:c.464G>A NP_000200.1:p.Arg155His
XR_941579.1:n.2190G>A
XR_941580.1:n.1106G>A
XR_941580.2:n.1118G>A
NM_000209.4:c.464G>A MANE Select NP_000200.1:p.Arg155His
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