Canonical Allele Identifier: CA483175665

Linked Data

MyVariant Identifiers: chr13:g.28494410G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920273G>T , CM000675.2:g.27920273G>T GRCh38
NC_000013.10:g.28494410G>T , CM000675.1:g.28494410G>T GRCh37
NC_000013.9:g.27392410G>T NCBI36
NG_008183.1:g.5243G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.135G>T (PDX1) MANE Select ENSP00000370421.4:p.Pro45=
ENST00000381033.4:c.135G>T (PDX1) ENSP00000370421.4:p.Pro45=
NM_000209.3:c.135G>T (PDX1) NP_000200.1:p.Pro45=
NR_047484.1:n.241+891C>A (PLUT)
XR_941578.1:n.280G>T (PDX1)
XR_941579.1:n.280G>T (PDX1)
XR_941580.1:n.280G>T (PDX1)
XR_941578.2:n.292G>T (PDX1)
XR_941580.2:n.292G>T (PDX1)
NM_000209.4:c.135G>T (PDX1) MANE Select NP_000200.1:p.Pro45=