Canonical Allele Identifier: CA2080721436
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924722C= , CM000675.2:g.27924722C= GRCh38
NC_000013.10:g.28498859C= , CM000675.1:g.28498859C= GRCh37
NC_000013.9:g.27396859C= NCBI36
NG_008183.1:g.9692C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*21C= MANE Select ENSP00000370421.4:n.*21C=
ENST00000381033.4:c.*21C= ENSP00000370421.4:n.*21C=
NM_000209.3:c.*21C= NP_000200.1:n.*21C=
NM_000209.4:c.*21C= MANE Select NP_000200.1:n.*21C=