Canonical Allele Identifier: CA387645407
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924331T>C , CM000675.2:g.27924331T>C GRCh38
NC_000013.10:g.28498468T>C , CM000675.1:g.28498468T>C GRCh37
NC_000013.9:g.27396468T>C NCBI36
NG_008183.1:g.9301T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.482T>C MANE Select ENSP00000370421.4:p.Leu161Pro
ENST00000381033.4:c.482T>C ENSP00000370421.4:p.Leu161Pro
NM_000209.3:c.482T>C NP_000200.1:p.Leu161Pro
XR_941580.1:n.1124T>C
XR_941580.2:n.1136T>C
NM_000209.4:c.482T>C MANE Select NP_000200.1:p.Leu161Pro