Canonical Allele Identifier: CA387645411
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924333G>T , CM000675.2:g.27924333G>T GRCh38
NC_000013.10:g.28498470G>T , CM000675.1:g.28498470G>T GRCh37
NC_000013.9:g.27396470G>T NCBI36
NG_008183.1:g.9303G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.484G>T MANE Select ENSP00000370421.4:p.Glu162Ter
ENST00000381033.4:c.484G>T ENSP00000370421.4:p.Glu162Ter
NM_000209.3:c.484G>T NP_000200.1:p.Glu162Ter
XR_941580.1:n.1126G>T
XR_941580.2:n.1138G>T
NM_000209.4:c.484G>T MANE Select NP_000200.1:p.Glu162Ter