Canonical Allele Identifier: CA2080721185
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924241C= , CM000675.2:g.27924241C= GRCh38
NC_000013.10:g.28498378C= , CM000675.1:g.28498378C= GRCh37
NC_000013.9:g.27396378C= NCBI36
NG_008183.1:g.9211C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-15C= MANE Select ENSP00000370421.4:n.407-15C=
ENST00000381033.4:c.407-15C= ENSP00000370421.4:n.407-15C=
NM_000209.3:c.407-15C= NP_000200.1:n.407-15C=
XR_941578.1:n.3534-15C=
XR_941579.1:n.2133-15C=
XR_941580.1:n.1049-15C=
XR_941578.2:n.3546-15C=
XR_941580.2:n.1061-15C=
NM_000209.4:c.407-15C= MANE Select NP_000200.1:n.407-15C=