Canonical Allele Identifier: CA2080721225
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924315G= , CM000675.2:g.27924315G= GRCh38
NC_000013.10:g.28498452G= , CM000675.1:g.28498452G= GRCh37
NC_000013.9:g.27396452G= NCBI36
NG_008183.1:g.9285G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.466G= MANE Select ENSP00000370421.4:p.Ala156=
ENST00000381033.4:c.466G= ENSP00000370421.4:p.Ala156=
NM_000209.3:c.466G= NP_000200.1:p.Ala156=
XR_941579.1:n.2192G=
XR_941580.1:n.1108G=
XR_941580.2:n.1120G=
NM_000209.4:c.466G= MANE Select NP_000200.1:p.Ala156=