Canonical Allele Identifier: CA2080721312
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924521G= , CM000675.2:g.27924521G= GRCh38
NC_000013.10:g.28498658G= , CM000675.1:g.28498658G= GRCh37
NC_000013.9:g.27396658G= NCBI36
NG_008183.1:g.9491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.672G= MANE Select ENSP00000370421.4:p.Glu224=
ENST00000381033.4:c.672G= ENSP00000370421.4:p.Glu224=
NM_000209.3:c.672G= NP_000200.1:p.Glu224=
NM_000209.4:c.672G= MANE Select NP_000200.1:p.Glu224=