Canonical Allele Identifier: CA387645268
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924264T>G , CM000675.2:g.27924264T>G GRCh38
NC_000013.10:g.28498401T>G , CM000675.1:g.28498401T>G GRCh37
NC_000013.9:g.27396401T>G NCBI36
NG_008183.1:g.9234T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.415T>G MANE Select ENSP00000370421.4:p.Tyr139Asp
ENST00000381033.4:c.415T>G ENSP00000370421.4:p.Tyr139Asp
NM_000209.3:c.415T>G NP_000200.1:p.Tyr139Asp
XR_941578.1:n.3542T>G
XR_941579.1:n.2141T>G
XR_941580.1:n.1057T>G
XR_941578.2:n.3554T>G
XR_941580.2:n.1069T>G
NM_000209.4:c.415T>G MANE Select NP_000200.1:p.Tyr139Asp