Canonical Allele Identifier: CA387645399
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924328A>C , CM000675.2:g.27924328A>C GRCh38
NC_000013.10:g.28498465A>C , CM000675.1:g.28498465A>C GRCh37
NC_000013.9:g.27396465A>C NCBI36
NG_008183.1:g.9298A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.479A>C MANE Select ENSP00000370421.4:p.Glu160Ala
ENST00000381033.4:c.479A>C ENSP00000370421.4:p.Glu160Ala
NM_000209.3:c.479A>C NP_000200.1:p.Glu160Ala
XR_941580.1:n.1121A>C
XR_941580.2:n.1133A>C
NM_000209.4:c.479A>C MANE Select NP_000200.1:p.Glu160Ala