Canonical Allele Identifier: CA2080721201
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924269T= , CM000675.2:g.27924269T= GRCh38
NC_000013.10:g.28498406T= , CM000675.1:g.28498406T= GRCh37
NC_000013.9:g.27396406T= NCBI36
NG_008183.1:g.9239T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.420T= MANE Select ENSP00000370421.4:p.Ala140=
ENST00000381033.4:c.420T= ENSP00000370421.4:p.Ala140=
NM_000209.3:c.420T= NP_000200.1:p.Ala140=
XR_941578.1:n.3547T=
XR_941579.1:n.2146T=
XR_941580.1:n.1062T=
XR_941578.2:n.3559T=
XR_941580.2:n.1074T=
NM_000209.4:c.420T= MANE Select NP_000200.1:p.Ala140=