Canonical Allele Identifier: CA483175644
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498466G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924329G>A , CM000675.2:g.27924329G>A GRCh38
NC_000013.10:g.28498466G>A , CM000675.1:g.28498466G>A GRCh37
NC_000013.9:g.27396466G>A NCBI36
NG_008183.1:g.9299G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.480G>A MANE Select ENSP00000370421.4:p.Glu160=
ENST00000381033.4:c.480G>A ENSP00000370421.4:p.Glu160=
NM_000209.3:c.480G>A NP_000200.1:p.Glu160=
XR_941580.1:n.1122G>A
XR_941580.2:n.1134G>A
NM_000209.4:c.480G>A MANE Select NP_000200.1:p.Glu160=