Canonical Allele Identifier: CA2080721269
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924436A= , CM000675.2:g.27924436A= GRCh38
NC_000013.10:g.28498573A= , CM000675.1:g.28498573A= GRCh37
NC_000013.9:g.27396573A= NCBI36
NG_008183.1:g.9406A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.587A= MANE Select ENSP00000370421.4:p.Asn196=
ENST00000381033.4:c.587A= ENSP00000370421.4:p.Asn196=
NM_000209.3:c.587A= NP_000200.1:p.Asn196=
NM_000209.4:c.587A= MANE Select NP_000200.1:p.Asn196=