Canonical Allele Identifier: CA387645438
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924344C>A , CM000675.2:g.27924344C>A GRCh38
NC_000013.10:g.28498481C>A , CM000675.1:g.28498481C>A GRCh37
NC_000013.9:g.27396481C>A NCBI36
NG_008183.1:g.9314C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.495C>A MANE Select ENSP00000370421.4:p.Phe165Leu
ENST00000381033.4:c.495C>A ENSP00000370421.4:p.Phe165Leu
NM_000209.3:c.495C>A NP_000200.1:p.Phe165Leu
NM_000209.4:c.495C>A MANE Select NP_000200.1:p.Phe165Leu