Canonical Allele Identifier: CA483175585

Linked Data

MyVariant Identifiers: chr13:g.28494365C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920228C>T , CM000675.2:g.27920228C>T GRCh38
NC_000013.10:g.28494365C>T , CM000675.1:g.28494365C>T GRCh37
NC_000013.9:g.27392365C>T NCBI36
NG_008183.1:g.5198C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.90C>T (PDX1) MANE Select ENSP00000370421.4:p.Ala30=
ENST00000381033.4:c.90C>T (PDX1) ENSP00000370421.4:p.Ala30=
NM_000209.3:c.90C>T (PDX1) NP_000200.1:p.Ala30=
NR_047484.1:n.241+936G>A (PLUT)
XR_941578.1:n.235C>T (PDX1)
XR_941579.1:n.235C>T (PDX1)
XR_941580.1:n.235C>T (PDX1)
XR_941578.2:n.247C>T (PDX1)
XR_941580.2:n.247C>T (PDX1)
NM_000209.4:c.90C>T (PDX1) MANE Select NP_000200.1:p.Ala30=