Canonical Allele Identifier: CA2080721186
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924242T= , CM000675.2:g.27924242T= GRCh38
NC_000013.10:g.28498379T= , CM000675.1:g.28498379T= GRCh37
NC_000013.9:g.27396379T= NCBI36
NG_008183.1:g.9212T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.407-14T= MANE Select ENSP00000370421.4:n.407-14T=
ENST00000381033.4:c.407-14T= ENSP00000370421.4:n.407-14T=
NM_000209.3:c.407-14T= NP_000200.1:n.407-14T=
XR_941578.1:n.3534-14T=
XR_941579.1:n.2133-14T=
XR_941580.1:n.1049-14T=
XR_941578.2:n.3546-14T=
XR_941580.2:n.1061-14T=
NM_000209.4:c.407-14T= MANE Select NP_000200.1:n.407-14T=