Canonical Allele Identifier: CA2080719098

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920367C= , CM000675.2:g.27920367C= GRCh38
NC_000013.10:g.28494504C= , CM000675.1:g.28494504C= GRCh37
NC_000013.9:g.27392504C= NCBI36
NG_008183.1:g.5337C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.229C= (PDX1) MANE Select ENSP00000370421.4:p.Pro77=
ENST00000381033.4:c.229C= (PDX1) ENSP00000370421.4:p.Pro77=
NM_000209.3:c.229C= (PDX1) NP_000200.1:p.Pro77=
NR_047484.1:n.241+797G= (PLUT)
XR_941578.1:n.374C= (PDX1)
XR_941579.1:n.374C= (PDX1)
XR_941580.1:n.374C= (PDX1)
XR_941578.2:n.386C= (PDX1)
XR_941580.2:n.386C= (PDX1)
NM_000209.4:c.229C= (PDX1) MANE Select NP_000200.1:p.Pro77=