Canonical Allele Identifier: CA2080721257
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924394T= , CM000675.2:g.27924394T= GRCh38
NC_000013.10:g.28498531T= , CM000675.1:g.28498531T= GRCh37
NC_000013.9:g.27396531T= NCBI36
NG_008183.1:g.9364T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.545T= MANE Select ENSP00000370421.4:p.Met182=
ENST00000381033.4:c.545T= ENSP00000370421.4:p.Met182=
NM_000209.3:c.545T= NP_000200.1:p.Met182=
NM_000209.4:c.545T= MANE Select NP_000200.1:p.Met182=