Canonical Allele Identifier: CA387645358
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924307A>T , CM000675.2:g.27924307A>T GRCh38
NC_000013.10:g.28498444A>T , CM000675.1:g.28498444A>T GRCh37
NC_000013.9:g.27396444A>T NCBI36
NG_008183.1:g.9277A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.458A>T MANE Select ENSP00000370421.4:p.Tyr153Phe
ENST00000381033.4:c.458A>T ENSP00000370421.4:p.Tyr153Phe
NM_000209.3:c.458A>T NP_000200.1:p.Tyr153Phe
XR_941579.1:n.2184A>T
XR_941580.1:n.1100A>T
XR_941580.2:n.1112A>T
NM_000209.4:c.458A>T MANE Select NP_000200.1:p.Tyr153Phe