Canonical Allele Identifier: CA2080721193
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924250C= , CM000675.2:g.27924250C= GRCh38
NC_000013.10:g.28498387C= , CM000675.1:g.28498387C= GRCh37
NC_000013.9:g.27396387C= NCBI36
NG_008183.1:g.9220C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.407-6C= MANE Select ENSP00000370421.4:n.407-6C=
ENST00000381033.4:c.407-6C= ENSP00000370421.4:n.407-6C=
NM_000209.3:c.407-6C= NP_000200.1:n.407-6C=
XR_941578.1:n.3534-6C=
XR_941579.1:n.2133-6C=
XR_941580.1:n.1049-6C=
XR_941578.2:n.3546-6C=
XR_941580.2:n.1061-6C=
NM_000209.4:c.407-6C= MANE Select NP_000200.1:n.407-6C=