Canonical Allele Identifier: CA387646143
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924474C>A , CM000675.2:g.27924474C>A GRCh38
NC_000013.10:g.28498611C>A , CM000675.1:g.28498611C>A GRCh37
NC_000013.9:g.27396611C>A NCBI36
NG_008183.1:g.9444C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.625C>A MANE Select ENSP00000370421.4:p.Arg209Ser
ENST00000381033.4:c.625C>A ENSP00000370421.4:p.Arg209Ser
NM_000209.3:c.625C>A NP_000200.1:p.Arg209Ser
NM_000209.4:c.625C>A MANE Select NP_000200.1:p.Arg209Ser