Canonical Allele Identifier: CA387645285
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924273G>C , CM000675.2:g.27924273G>C GRCh38
NC_000013.10:g.28498410G>C , CM000675.1:g.28498410G>C GRCh37
NC_000013.9:g.27396410G>C NCBI36
NG_008183.1:g.9243G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.424G>C MANE Select ENSP00000370421.4:p.Glu142Gln
ENST00000381033.4:c.424G>C ENSP00000370421.4:p.Glu142Gln
NM_000209.3:c.424G>C NP_000200.1:p.Glu142Gln
XR_941578.1:n.3551G>C
XR_941579.1:n.2150G>C
XR_941580.1:n.1066G>C
XR_941578.2:n.3563G>C
XR_941580.2:n.1078G>C
NM_000209.4:c.424G>C MANE Select NP_000200.1:p.Glu142Gln