Canonical Allele Identifier: CA2080721227
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924317A= , CM000675.2:g.27924317A= GRCh38
NC_000013.10:g.28498454A= , CM000675.1:g.28498454A= GRCh37
NC_000013.9:g.27396454A= NCBI36
NG_008183.1:g.9287A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.468A= MANE Select ENSP00000370421.4:p.Ala156=
ENST00000381033.4:c.468A= ENSP00000370421.4:p.Ala156=
NM_000209.3:c.468A= NP_000200.1:p.Ala156=
XR_941580.1:n.1110A=
XR_941580.2:n.1122A=
NM_000209.4:c.468A= MANE Select NP_000200.1:p.Ala156=