Canonical Allele Identifier: CA2080721200
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924267G= , CM000675.2:g.27924267G= GRCh38
NC_000013.10:g.28498404G= , CM000675.1:g.28498404G= GRCh37
NC_000013.9:g.27396404G= NCBI36
NG_008183.1:g.9237G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.418G= MANE Select ENSP00000370421.4:p.Ala140=
ENST00000381033.4:c.418G= ENSP00000370421.4:p.Ala140=
NM_000209.3:c.418G= NP_000200.1:p.Ala140=
XR_941578.1:n.3545G=
XR_941579.1:n.2144G=
XR_941580.1:n.1060G=
XR_941578.2:n.3557G=
XR_941580.2:n.1072G=
NM_000209.4:c.418G= MANE Select NP_000200.1:p.Ala140=