Canonical Allele Identifier: CA2080719092

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920364G= , CM000675.2:g.27920364G= GRCh38
NC_000013.10:g.28494501G= , CM000675.1:g.28494501G= GRCh37
NC_000013.9:g.27392501G= NCBI36
NG_008183.1:g.5334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.226G= (PDX1) MANE Select ENSP00000370421.4:p.Asp76=
ENST00000381033.4:c.226G= (PDX1) ENSP00000370421.4:p.Asp76=
NM_000209.3:c.226G= (PDX1) NP_000200.1:p.Asp76=
NR_047484.1:n.241+800C= (PLUT)
XR_941578.1:n.371G= (PDX1)
XR_941579.1:n.371G= (PDX1)
XR_941580.1:n.371G= (PDX1)
XR_941578.2:n.383G= (PDX1)
XR_941580.2:n.383G= (PDX1)
NM_000209.4:c.226G= (PDX1) MANE Select NP_000200.1:p.Asp76=