Canonical Allele Identifier: CA387643399

Linked Data

dbSNP Id: rs936474667

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920166G>T , CM000675.2:g.27920166G>T GRCh38
NC_000013.10:g.28494303G>T , CM000675.1:g.28494303G>T GRCh37
NC_000013.9:g.27392303G>T NCBI36
NG_008183.1:g.5136G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.28G>T (PDX1) MANE Select ENSP00000370421.4:p.Ala10Ser
ENST00000381033.4:c.28G>T (PDX1) ENSP00000370421.4:p.Ala10Ser
NM_000209.3:c.28G>T (PDX1) NP_000200.1:p.Ala10Ser
NR_047484.1:n.241+998C>A (PLUT)
XR_941578.1:n.173G>T (PDX1)
XR_941579.1:n.173G>T (PDX1)
XR_941580.1:n.173G>T (PDX1)
XR_941578.2:n.185G>T (PDX1)
XR_941580.2:n.185G>T (PDX1)
NM_000209.4:c.28G>T (PDX1) MANE Select NP_000200.1:p.Ala10Ser