Canonical Allele Identifier: CA387646983
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924699T>A , CM000675.2:g.27924699T>A GRCh38
NC_000013.10:g.28498836T>A , CM000675.1:g.28498836T>A GRCh37
NC_000013.9:g.27396836T>A NCBI36
NG_008183.1:g.9669T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.850T>A MANE Select ENSP00000370421.4:p.Ter284Arg
ENST00000381033.4:c.850T>A ENSP00000370421.4:p.Ter284Arg
NM_000209.3:c.850T>A NP_000200.1:p.Ter284Arg
NM_000209.4:c.850T>A MANE Select NP_000200.1:p.Ter284Arg