Canonical Allele Identifier: CA483175784

Linked Data

MyVariant Identifiers: chr13:g.28494512G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920375G>C , CM000675.2:g.27920375G>C GRCh38
NC_000013.10:g.28494512G>C , CM000675.1:g.28494512G>C GRCh37
NC_000013.9:g.27392512G>C NCBI36
NG_008183.1:g.5345G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.237G>C (PDX1) MANE Select ENSP00000370421.4:p.Val79=
ENST00000381033.4:c.237G>C (PDX1) ENSP00000370421.4:p.Val79=
NM_000209.3:c.237G>C (PDX1) NP_000200.1:p.Val79=
NR_047484.1:n.241+789C>G (PLUT)
XR_941578.1:n.382G>C (PDX1)
XR_941579.1:n.382G>C (PDX1)
XR_941580.1:n.382G>C (PDX1)
XR_941578.2:n.394G>C (PDX1)
XR_941580.2:n.394G>C (PDX1)
NM_000209.4:c.237G>C (PDX1) MANE Select NP_000200.1:p.Val79=