Canonical Allele Identifier: CA387645388
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924322T>A , CM000675.2:g.27924322T>A GRCh38
NC_000013.10:g.28498459T>A , CM000675.1:g.28498459T>A GRCh37
NC_000013.9:g.27396459T>A NCBI36
NG_008183.1:g.9292T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.473T>A MANE Select ENSP00000370421.4:p.Leu158Gln
ENST00000381033.4:c.473T>A ENSP00000370421.4:p.Leu158Gln
NM_000209.3:c.473T>A NP_000200.1:p.Leu158Gln
XR_941580.1:n.1115T>A
XR_941580.2:n.1127T>A
NM_000209.4:c.473T>A MANE Select NP_000200.1:p.Leu158Gln