Canonical Allele Identifier: CA2080718778

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920237T= , CM000675.2:g.27920237T= GRCh38
NC_000013.10:g.28494374T= , CM000675.1:g.28494374T= GRCh37
NC_000013.9:g.27392374T= NCBI36
NG_008183.1:g.5207T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.99T= (PDX1) MANE Select ENSP00000370421.4:p.Pro33=
ENST00000381033.4:c.99T= (PDX1) ENSP00000370421.4:p.Pro33=
NM_000209.3:c.99T= (PDX1) NP_000200.1:p.Pro33=
NR_047484.1:n.241+927A= (PLUT)
XR_941578.1:n.244T= (PDX1)
XR_941579.1:n.244T= (PDX1)
XR_941580.1:n.244T= (PDX1)
XR_941578.2:n.256T= (PDX1)
XR_941580.2:n.256T= (PDX1)
NM_000209.4:c.99T= (PDX1) MANE Select NP_000200.1:p.Pro33=