Canonical Allele Identifier: CA387643837

Linked Data

dbSNP Id: rs1340060753

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920232C>G , CM000675.2:g.27920232C>G GRCh38
NC_000013.10:g.28494369C>G , CM000675.1:g.28494369C>G GRCh37
NC_000013.9:g.27392369C>G NCBI36
NG_008183.1:g.5202C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.94C>G (PDX1) MANE Select ENSP00000370421.4:p.Pro32Ala
ENST00000381033.4:c.94C>G (PDX1) ENSP00000370421.4:p.Pro32Ala
NM_000209.3:c.94C>G (PDX1) NP_000200.1:p.Pro32Ala
NR_047484.1:n.241+932G>C (PLUT)
XR_941578.1:n.239C>G (PDX1)
XR_941579.1:n.239C>G (PDX1)
XR_941580.1:n.239C>G (PDX1)
XR_941578.2:n.251C>G (PDX1)
XR_941580.2:n.251C>G (PDX1)
NM_000209.4:c.94C>G (PDX1) MANE Select NP_000200.1:p.Pro32Ala