Canonical Allele Identifier: CA2080721450
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924763T= , CM000675.2:g.27924763T= GRCh38
NC_000013.10:g.28498900T= , CM000675.1:g.28498900T= GRCh37
NC_000013.9:g.27396900T= NCBI36
NG_008183.1:g.9733T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*62T= MANE Select ENSP00000370421.4:n.*62T=
ENST00000381033.4:c.*62T= ENSP00000370421.4:n.*62T=
NM_000209.3:c.*62T= NP_000200.1:n.*62T=
NM_000209.4:c.*62T= MANE Select NP_000200.1:n.*62T=