Canonical Allele Identifier: CA2080721198
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924263C= , CM000675.2:g.27924263C= GRCh38
NC_000013.10:g.28498400C= , CM000675.1:g.28498400C= GRCh37
NC_000013.9:g.27396400C= NCBI36
NG_008183.1:g.9233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.414C= MANE Select ENSP00000370421.4:p.Ala138=
ENST00000381033.4:c.414C= ENSP00000370421.4:p.Ala138=
NM_000209.3:c.414C= NP_000200.1:p.Ala138=
XR_941578.1:n.3541C=
XR_941579.1:n.2140C=
XR_941580.1:n.1056C=
XR_941578.2:n.3553C=
XR_941580.2:n.1068C=
NM_000209.4:c.414C= MANE Select NP_000200.1:p.Ala138=