Canonical Allele Identifier: CA325742
Community Standard Title: NM_000209.4(PDX1):c.-18C>T

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920121C>T , CM000675.2:g.27920121C>T GRCh38
NC_000013.10:g.28494258C>T , CM000675.1:g.28494258C>T GRCh37
NC_000013.9:g.27392258C>T NCBI36
NG_008183.1:g.5091C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000209.4:c.-18C>T (PDX1) MANE Select NP_000200.1:n.-18C>T
ENST00000381033.5:c.-18C>T (PDX1) MANE Select ENSP00000370421.4:n.-18C>T
NM_000209.3:c.-18C>T (PDX1) NP_000200.1:n.-18C>T
NR_047484.1:n.241+1043G>A (PLUT)
ENST00000381033.4:c.-18C>T (PDX1) ENSP00000370421.4:n.-18C>T
XR_941578.1:n.128C>T (PDX1)
XR_941578.2:n.140C>T (PDX1)
XR_941579.1:n.128C>T (PDX1)
XR_941580.1:n.128C>T (PDX1)
XR_941580.2:n.140C>T (PDX1)