Canonical Allele Identifier: CA387645392
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924324C>G , CM000675.2:g.27924324C>G GRCh38
NC_000013.10:g.28498461C>G , CM000675.1:g.28498461C>G GRCh37
NC_000013.9:g.27396461C>G NCBI36
NG_008183.1:g.9294C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.475C>G MANE Select ENSP00000370421.4:p.Leu159Val
ENST00000381033.4:c.475C>G ENSP00000370421.4:p.Leu159Val
NM_000209.3:c.475C>G NP_000200.1:p.Leu159Val
XR_941580.1:n.1117C>G
XR_941580.2:n.1129C>G
NM_000209.4:c.475C>G MANE Select NP_000200.1:p.Leu159Val