Canonical Allele Identifier: CA2080721271
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924439G= , CM000675.2:g.27924439G= GRCh38
NC_000013.10:g.28498576G= , CM000675.1:g.28498576G= GRCh37
NC_000013.9:g.27396576G= NCBI36
NG_008183.1:g.9409G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.590G= MANE Select ENSP00000370421.4:p.Arg197=
ENST00000381033.4:c.590G= ENSP00000370421.4:p.Arg197=
NM_000209.3:c.590G= NP_000200.1:p.Arg197=
NM_000209.4:c.590G= MANE Select NP_000200.1:p.Arg197=