Canonical Allele Identifier: CA387645378
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498455C>A (hg19) chr13:g.27924318C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924318C>A , CM000675.2:g.27924318C>A GRCh38
NC_000013.10:g.28498455C>A , CM000675.1:g.28498455C>A GRCh37
NC_000013.9:g.27396455C>A NCBI36
NG_008183.1:g.9288C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.469C>A MANE Select ENSP00000370421.4:p.Gln157Lys
ENST00000381033.4:c.469C>A ENSP00000370421.4:p.Gln157Lys
NM_000209.3:c.469C>A NP_000200.1:p.Gln157Lys
XR_941580.1:n.1111C>A
XR_941580.2:n.1123C>A
NM_000209.4:c.469C>A MANE Select NP_000200.1:p.Gln157Lys
Search 100 bp 5'
Search 100 bp 3'