Canonical Allele Identifier: CA387646777
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924648G>A , CM000675.2:g.27924648G>A GRCh38
NC_000013.10:g.28498785G>A , CM000675.1:g.28498785G>A GRCh37
NC_000013.9:g.27396785G>A NCBI36
NG_008183.1:g.9618G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.799G>A MANE Select ENSP00000370421.4:p.Ala267Thr
ENST00000381033.4:c.799G>A ENSP00000370421.4:p.Ala267Thr
NM_000209.3:c.799G>A NP_000200.1:p.Ala267Thr
NM_000209.4:c.799G>A MANE Select NP_000200.1:p.Ala267Thr