Canonical Allele Identifier: CA2080721249
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924382A= , CM000675.2:g.27924382A= GRCh38
NC_000013.10:g.28498519A= , CM000675.1:g.28498519A= GRCh37
NC_000013.9:g.27396519A= NCBI36
NG_008183.1:g.9352A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.533A= MANE Select ENSP00000370421.4:p.Glu178=
ENST00000381033.4:c.533A= ENSP00000370421.4:p.Glu178=
NM_000209.3:c.533A= NP_000200.1:p.Glu178=
NM_000209.4:c.533A= MANE Select NP_000200.1:p.Glu178=