Canonical Allele Identifier: CA387643824
Gene: PDX1 HGNC NCBI
PLUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28494366A>C (hg19) chr13:g.27920229A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920229A>C , CM000675.2:g.27920229A>C GRCh38
NC_000013.10:g.28494366A>C , CM000675.1:g.28494366A>C GRCh37
NC_000013.9:g.27392366A>C NCBI36
NG_008183.1:g.5199A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.91A>C (PDX1) MANE Select ENSP00000370421.4:p.Ser31Arg
ENST00000381033.4:c.91A>C (PDX1) ENSP00000370421.4:p.Ser31Arg
NM_000209.3:c.91A>C (PDX1) NP_000200.1:p.Ser31Arg
NR_047484.1:n.241+935T>G (PLUT)
XR_941578.1:n.236A>C (PDX1)
XR_941579.1:n.236A>C (PDX1)
XR_941580.1:n.236A>C (PDX1)
XR_941578.2:n.248A>C (PDX1)
XR_941580.2:n.248A>C (PDX1)
NM_000209.4:c.91A>C (PDX1) MANE Select NP_000200.1:p.Ser31Arg
Search 100 bp 5'
Search 100 bp 3'