Canonical Allele Identifier: CA2080721410
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924677T= , CM000675.2:g.27924677T= GRCh38
NC_000013.10:g.28498814T= , CM000675.1:g.28498814T= GRCh37
NC_000013.9:g.27396814T= NCBI36
NG_008183.1:g.9647T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.828T= MANE Select ENSP00000370421.4:p.Pro276=
ENST00000381033.4:c.828T= ENSP00000370421.4:p.Pro276=
NM_000209.3:c.828T= NP_000200.1:p.Pro276=
NM_000209.4:c.828T= MANE Select NP_000200.1:p.Pro276=