Canonical Allele Identifier: CA2080721176
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924228C= , CM000675.2:g.27924228C= GRCh38
NC_000013.10:g.28498365C= , CM000675.1:g.28498365C= GRCh37
NC_000013.9:g.27396365C= NCBI36
NG_008183.1:g.9198C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-28C= MANE Select ENSP00000370421.4:n.407-28C=
ENST00000381033.4:c.407-28C= ENSP00000370421.4:n.407-28C=
NM_000209.3:c.407-28C= NP_000200.1:n.407-28C=
XR_941578.1:n.3534-28C=
XR_941579.1:n.2133-28C=
XR_941580.1:n.1049-28C=
XR_941578.2:n.3546-28C=
XR_941580.2:n.1061-28C=
NM_000209.4:c.407-28C= MANE Select NP_000200.1:n.407-28C=