Canonical Allele Identifier: CA2080721233
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924342T= , CM000675.2:g.27924342T= GRCh38
NC_000013.10:g.28498479T= , CM000675.1:g.28498479T= GRCh37
NC_000013.9:g.27396479T= NCBI36
NG_008183.1:g.9312T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.493T= MANE Select ENSP00000370421.4:p.Phe165=
ENST00000381033.4:c.493T= ENSP00000370421.4:p.Phe165=
NM_000209.3:c.493T= NP_000200.1:p.Phe165=
NM_000209.4:c.493T= MANE Select NP_000200.1:p.Phe165=