Canonical Allele Identifier: CA2080721226
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924316C= , CM000675.2:g.27924316C= GRCh38
NC_000013.10:g.28498453C= , CM000675.1:g.28498453C= GRCh37
NC_000013.9:g.27396453C= NCBI36
NG_008183.1:g.9286C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.467C= MANE Select ENSP00000370421.4:p.Ala156=
ENST00000381033.4:c.467C= ENSP00000370421.4:p.Ala156=
NM_000209.3:c.467C= NP_000200.1:p.Ala156=
XR_941580.1:n.1109C=
XR_941580.2:n.1121C=
NM_000209.4:c.467C= MANE Select NP_000200.1:p.Ala156=