Canonical Allele Identifier: CA483175664

Linked Data

MyVariant Identifiers: chr13:g.28494407G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920270G>T , CM000675.2:g.27920270G>T GRCh38
NC_000013.10:g.28494407G>T , CM000675.1:g.28494407G>T GRCh37
NC_000013.9:g.27392407G>T NCBI36
NG_008183.1:g.5240G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.132G>T (PDX1) MANE Select ENSP00000370421.4:p.Pro44=
ENST00000381033.4:c.132G>T (PDX1) ENSP00000370421.4:p.Pro44=
NM_000209.3:c.132G>T (PDX1) NP_000200.1:p.Pro44=
NR_047484.1:n.241+894C>A (PLUT)
XR_941578.1:n.277G>T (PDX1)
XR_941579.1:n.277G>T (PDX1)
XR_941580.1:n.277G>T (PDX1)
XR_941578.2:n.289G>T (PDX1)
XR_941580.2:n.289G>T (PDX1)
NM_000209.4:c.132G>T (PDX1) MANE Select NP_000200.1:p.Pro44=