Canonical Allele Identifier: CA387645395
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924325T>G , CM000675.2:g.27924325T>G GRCh38
NC_000013.10:g.28498462T>G , CM000675.1:g.28498462T>G GRCh37
NC_000013.9:g.27396462T>G NCBI36
NG_008183.1:g.9295T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.476T>G MANE Select ENSP00000370421.4:p.Leu159Arg
ENST00000381033.4:c.476T>G ENSP00000370421.4:p.Leu159Arg
NM_000209.3:c.476T>G NP_000200.1:p.Leu159Arg
XR_941580.1:n.1118T>G
XR_941580.2:n.1130T>G
NM_000209.4:c.476T>G MANE Select NP_000200.1:p.Leu159Arg