Canonical Allele Identifier: CA2080718838

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920264C= , CM000675.2:g.27920264C= GRCh38
NC_000013.10:g.28494401C= , CM000675.1:g.28494401C= GRCh37
NC_000013.9:g.27392401C= NCBI36
NG_008183.1:g.5234C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.126C= (PDX1) MANE Select ENSP00000370421.4:p.Pro42=
ENST00000381033.4:c.126C= (PDX1) ENSP00000370421.4:p.Pro42=
NM_000209.3:c.126C= (PDX1) NP_000200.1:p.Pro42=
NR_047484.1:n.241+900G= (PLUT)
XR_941578.1:n.271C= (PDX1)
XR_941579.1:n.271C= (PDX1)
XR_941580.1:n.271C= (PDX1)
XR_941578.2:n.283C= (PDX1)
XR_941580.2:n.283C= (PDX1)
NM_000209.4:c.126C= (PDX1) MANE Select NP_000200.1:p.Pro42=