Canonical Allele Identifier: CA387643329

Linked Data

dbSNP Id: rs1857771781

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920158A>C , CM000675.2:g.27920158A>C GRCh38
NC_000013.10:g.28494295A>C , CM000675.1:g.28494295A>C GRCh37
NC_000013.9:g.27392295A>C NCBI36
NG_008183.1:g.5128A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.20A>C (PDX1) MANE Select ENSP00000370421.4:p.Tyr7Ser
ENST00000381033.4:c.20A>C (PDX1) ENSP00000370421.4:p.Tyr7Ser
NM_000209.3:c.20A>C (PDX1) NP_000200.1:p.Tyr7Ser
NR_047484.1:n.241+1006T>G (PLUT)
XR_941578.1:n.165A>C (PDX1)
XR_941579.1:n.165A>C (PDX1)
XR_941580.1:n.165A>C (PDX1)
XR_941578.2:n.177A>C (PDX1)
XR_941580.2:n.177A>C (PDX1)
NM_000209.4:c.20A>C (PDX1) MANE Select NP_000200.1:p.Tyr7Ser