Canonical Allele Identifier: CA2080721196
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924260C= , CM000675.2:g.27924260C= GRCh38
NC_000013.10:g.28498397C= , CM000675.1:g.28498397C= GRCh37
NC_000013.9:g.27396397C= NCBI36
NG_008183.1:g.9230C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.411C= MANE Select ENSP00000370421.4:p.Gly137=
ENST00000381033.4:c.411C= ENSP00000370421.4:p.Gly137=
NM_000209.3:c.411C= NP_000200.1:p.Gly137=
XR_941578.1:n.3538C=
XR_941579.1:n.2137C=
XR_941580.1:n.1053C=
XR_941578.2:n.3550C=
XR_941580.2:n.1065C=
NM_000209.4:c.411C= MANE Select NP_000200.1:p.Gly137=