Canonical Allele Identifier: CA2080721331
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924550A= , CM000675.2:g.27924550A= GRCh38
NC_000013.10:g.28498687A= , CM000675.1:g.28498687A= GRCh37
NC_000013.9:g.27396687A= NCBI36
NG_008183.1:g.9520A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.701A= MANE Select ENSP00000370421.4:p.Glu234=
ENST00000381033.4:c.701A= ENSP00000370421.4:p.Glu234=
NM_000209.3:c.701A= NP_000200.1:p.Glu234=
NM_000209.4:c.701A= MANE Select NP_000200.1:p.Glu234=