Canonical Allele Identifier: CA387645413
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924334A>G , CM000675.2:g.27924334A>G GRCh38
NC_000013.10:g.28498471A>G , CM000675.1:g.28498471A>G GRCh37
NC_000013.9:g.27396471A>G NCBI36
NG_008183.1:g.9304A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.485A>G MANE Select ENSP00000370421.4:p.Glu162Gly
ENST00000381033.4:c.485A>G ENSP00000370421.4:p.Glu162Gly
NM_000209.3:c.485A>G NP_000200.1:p.Glu162Gly
XR_941580.1:n.1127A>G
XR_941580.2:n.1139A>G
NM_000209.4:c.485A>G MANE Select NP_000200.1:p.Glu162Gly