Canonical Allele Identifier: CA387643783

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920221T>G , CM000675.2:g.27920221T>G GRCh38
NC_000013.10:g.28494358T>G , CM000675.1:g.28494358T>G GRCh37
NC_000013.9:g.27392358T>G NCBI36
NG_008183.1:g.5191T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.83T>G (PDX1) MANE Select ENSP00000370421.4:p.Phe28Cys
ENST00000381033.4:c.83T>G (PDX1) ENSP00000370421.4:p.Phe28Cys
NM_000209.3:c.83T>G (PDX1) NP_000200.1:p.Phe28Cys
NR_047484.1:n.241+943A>C (PLUT)
XR_941578.1:n.228T>G (PDX1)
XR_941579.1:n.228T>G (PDX1)
XR_941580.1:n.228T>G (PDX1)
XR_941578.2:n.240T>G (PDX1)
XR_941580.2:n.240T>G (PDX1)
NM_000209.4:c.83T>G (PDX1) MANE Select NP_000200.1:p.Phe28Cys