Canonical Allele Identifier: CA387645398
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924327G>T , CM000675.2:g.27924327G>T GRCh38
NC_000013.10:g.28498464G>T , CM000675.1:g.28498464G>T GRCh37
NC_000013.9:g.27396464G>T NCBI36
NG_008183.1:g.9297G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.478G>T MANE Select ENSP00000370421.4:p.Glu160Ter
ENST00000381033.4:c.478G>T ENSP00000370421.4:p.Glu160Ter
NM_000209.3:c.478G>T NP_000200.1:p.Glu160Ter
XR_941580.1:n.1120G>T
XR_941580.2:n.1132G>T
NM_000209.4:c.478G>T MANE Select NP_000200.1:p.Glu160Ter