Canonical Allele Identifier: CA2080721295
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924496G= , CM000675.2:g.27924496G= GRCh38
NC_000013.10:g.28498633G= , CM000675.1:g.28498633G= GRCh37
NC_000013.9:g.27396633G= NCBI36
NG_008183.1:g.9466G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.647G= MANE Select ENSP00000370421.4:p.Gly216=
ENST00000381033.4:c.647G= ENSP00000370421.4:p.Gly216=
NM_000209.3:c.647G= NP_000200.1:p.Gly216=
NM_000209.4:c.647G= MANE Select NP_000200.1:p.Gly216=