Canonical Allele Identifier: CA2080721229
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924326A= , CM000675.2:g.27924326A= GRCh38
NC_000013.10:g.28498463A= , CM000675.1:g.28498463A= GRCh37
NC_000013.9:g.27396463A= NCBI36
NG_008183.1:g.9296A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.477A= MANE Select ENSP00000370421.4:p.Leu159=
ENST00000381033.4:c.477A= ENSP00000370421.4:p.Leu159=
NM_000209.3:c.477A= NP_000200.1:p.Leu159=
XR_941580.1:n.1119A=
XR_941580.2:n.1131A=
NM_000209.4:c.477A= MANE Select NP_000200.1:p.Leu159=